Some standard content:
ICS55.200
National Standard of the People's Republic of China
GB/T24570—2009
Aseptic bag forming-filling-sealing machine
Aseptic bag forming-filling-sealing machine2009-10-30 Issued
General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China Standardization Administration of China
2010-03-01 Implementation
This standard is proposed and managed by the National Technical Committee for Standardization of Packaging Machinery (SAC/TC436). GB/T24570—2009
The responsible drafting units of this standard are: Hangzhou Zhongya Machinery Co., Ltd. and the Quality Supervision and Inspection Center for Packaging Machinery Products of the Machinery Industry. The main drafters of this standard are: Shi Zheng, Ji Yonglin, Zhang Shuangman, Yu Limin and Chen Runjie. I
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Aseptic bag forming filling sealing machine
GB/T245702009
This standard specifies the terms and definitions, models, types, basic parameters and working conditions, requirements, test methods, inspection rules, marking, packaging, transportation and storage requirements of aseptic bag forming filling sealing machine (hereinafter referred to as "aseptic machine"). This standard applies to aseptic bag forming filling sealing machines for filling fresh milk, juice, milk beverages and other non-gas liquids, and is used in daily chemical, pharmaceutical, food and other industries.
2Normative references
The clauses in the following documents become the clauses of this standard through reference in this standard. For all dated referenced documents, all subsequent amendments (excluding errata) or revisions are not applicable to this standard. However, the parties to the agreement based on this standard are encouraged to study whether the latest versions of these documents can be used. For all undated referenced documents, the latest versions are applicable to this standard. GB/T191 Pictorial signs for packaging, storage and transportation (GB/T191-2008, ISO780:1997, MOD) GB2894 Safety signs and guidelines for their use
GB/T4789.2 Microbiological examination of food hygiene Determination of total colony count GB/T5048 Moisture-proof packaging
GB5226.1-2002 Safety of machinery Mechanical electrical equipment Part 1: General technical conditions (IEC60204-1:2000, IDT) GB5749 Hygienic standards for drinking water
GB/T7 311 Classification and model compilation method of packaging machinery GB9969 General principles for the manual of industrial products GB12073 Safety and sanitation of dairy equipment
GB/T13306 Signs
GB/T13384
General technical conditions for packaging of electromechanical products
GB16179 Guidelines for the use of safety signs
Graphical symbols for equipment Part 1: General symbols (GB/T16273.1-2008, ISO7000:2004, GB/T16273.1
GB/ T16292
GB/T16293
Test method for suspended particles in clean rooms (areas) for pharmaceutical industryTest method for floating bacteria in clean rooms (areas) for pharmaceutical industryTest method for settling bacteria in clean rooms (areas) for pharmaceutical industryGB/T16294
GB16798 Food machinery safety and sanitation
GB/T18883—2002 Indoor air quality standardGB19741
Safety and hygienic requirements for mechanical design of plastic composite films and bags for liquid food packaging (GB19891--20 05, ISO14159:2002, MOD) GB19891
JB/T7232 Simple method for determination of sound power level of packaging machinery noise JB7233 Safety requirements for packaging machinery
JJF1070 Rules for metrological inspection of net content of quantitatively packaged goods Ministry of Health of the People's Republic of China "Technical Specification for Disinfection" (2002 Edition) 3 Terms and definitions
The following terms and definitions apply to this standard. GB/T24570—2009
Commercial sterile
commercial sterilization
The packaged filling material does not contain pathogenic bacteria or microorganisms that can proliferate at room temperature. 3.2
Aseptic packaging
Aseptic packaging
Packaging and sealing of sterilized liquid food in sterilized containers under aseptic conditions, so that the food can be transported and stored at room temperature during the shelf life.
Class 100 clean room (area) Class 100 clean room (area) A room or area that is required to be environmentally controlled for dust particles and microbial contamination according to regulations, and its equipment, structure and use have the function of reducing the entry, generation and retention of pollution sources in the area. The cleanliness level of the clean room (area) meets the standards of the /00 clean room (area) specified in B/T16292, GB/T16293, and GB/T16294. 3.4
Ultra-high temperature instantaneous sterilization
heat treated, UHT
The sterilization process of heating the product to 120℃~150℃ in a closed system for 4s~30s and then rapidly cooling it to room temperature is referred to as "UHT".
Aseptic bag forming-filling-sealing machineAseptic bag forming-filling-sealing machineA machine that uses paper-based composite film CQ
Tech composite film, aluminum-plastic composite film, and plastic multi-layer co-extruded film as packaging materials to automatically complete forming, room temperature filling and sealing in a sterile environment.
Production capacity
Production capacity
The number of finished bags produced per unit time, in bags/h. When the aseptic machine is running stably
Average actual content
average actual quantity
The arithmetic mean of the actual quantity of the sample unitFilling precision
filling precision tolerance
The maximum allowable error of the amount of the filling material in the packaging container. Asepsis qualified rate
qualified asepsis ratio
Under the condition of normal UHT and the aseptic machine running stably, the percentage of the number of packages in the sampled finished packaging bags that have no bulging and the difference in pH value (compared with the pH value of the original material) is not more than 0.2 to the total number of packages inspected. 3.10
qualifiedpackage ratio
Qualified package ratio
Under the condition of qualified filling precision, the percentage of the number of packages that have passed the bag shape, appearance, heat sealing strength, static pressure and drop tests to the total number of packages inspected.
4 Model, type, basic parameters and working conditions 4.1 Model
The model of the aseptic machine shall be compiled in accordance with the provisions of GB/T7311. 2
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GB/T24570—2009
Improved design sequence code. It is represented by the English letters A and BC in sequence. The first design product has no sequence code. Derived sequence code: represented by Roman numerals I, Ⅱ, Ⅱ. Main parameters: production capacity (unit: bag/h)/1000. Structural type code: pneumatic (Q), ordinary transmission (P), servo (S). Aseptic bag forming filling and sealing machine.
Example: DXDW-Q6A means a pneumatically driven aseptic bag forming filling and sealing machine with a production capacity of 6000 bags/h, and the first improved design. 4.2 Types and basic parameters
4.2.1 Aseptic machines are divided into several types according to the following situations: a) According to the driving mode, they are divided into: pneumatic (Q), ordinary transmission (P), servo (S); b) According to the number of filling heads, they are divided into: single head, multiple heads. 4.2.2 Basic parameters:
The basic parameters of aseptic machines should include:
a) Packaging capacity: mL;
b) Packaging size: (length × width) mm;
Power: kW;
d) Working voltage and frequency: V, Hz;
Production capacity: The unit is bag/h.
4.3 Working conditions
4.3.1 Water (including sterile and aseptic), electricity, gas (including sterile and aseptic), compressed air (compressed air pressure ≥ 0.6MPa), steam (not less than 0.5MPa), disinfectant and other process conditions and parameters should all meet the requirements of aseptic machines. 4.3.2. The steam system and compressed air system should have safety devices. The main pipeline of the steam system should be insulated. The branch pipeline that is not convenient for insulation should have obvious high-temperature signs. The signs should comply with the provisions of GB2894. 4.3.3 The air compressor and its storage tank should be separated from the aseptic packaging workshop. 4.3.4 The production water should comply with the provisions of GB5749. 4.3.5 The packaging material should meet the food hygiene requirements, the bacterial count should be less than 10CFU/cm2, the packaging material should be oxygen-proof and light-proof, the melting point temperature should not be higher than 160℃, and the thickness should be 0.09mm~0.15mm. 4.3.6 The total bacterial count of the raw materials before UHT treatment shall not exceed 2×105CFU/mL. The matching pre-treatment equipment and ultra-high temperature instantaneous sterilization equipment (UHT) should meet the commercial sterility requirements, SE ≥ 9. 4.3.7
Note: SE represents sterilization efficiency, which refers to the logarithmic value of the ratio of the total number of microorganisms before and after sterilization of materials and equipment, SE-1og Linglei Mo Bio-meaning Number Total number of microorganisms before sterilization
4.3.8 The material pipelines and pipe fittings connected to the pre-matching treatment equipment should be made of food-grade stainless steel and should meet the requirements of GB12073.
4.3.9 The deviation between the power supply voltage and the rated voltage shall not exceed -10% and +5%. 4.3.10 Hydrogen peroxide should reach food grade, and the concentration shall not be less than 30% (volume fraction). 5 Requirements
5.1 The aseptic machine shall meet the requirements of this standard and be manufactured according to the drawings and technical documents approved by the prescribed procedures. 5.2 The aseptic machine shall operate smoothly, and the movement of the moving parts shall be sensitive, coordinated and accurate, without obstruction and abnormal sound. 5.3 The circuit control system of the sterile machine shall comply with the requirements of GB5226.1, be safe and reliable, and operate accurately. Each electrical connector shall be firmly connected and numbered; the operating button shall be flexible and have an emergency stop button; the indicator light display shall be normal. 5.4 The steam, compressed air, lubrication system, and conveying pipeline in the sterile machine shall be unobstructed, flexible to control, and leak-free, and comply with the relevant provisions of the national and industry standards GB/T24570-2009.
5.5 The production capacity of the sterile machine shall reach the rated production capacity. 5.6 The cleanliness of the clean area (room) shall meet the 100-level standard. The air flow shall flow from the high-level area to the adjacent low-level area. The high-level area shall maintain a positive pressure of 10Pa to 15Pa relative to the low-level area, and the monitoring of the positive pressure shall be continuous and visible. 5.7 The sterile machine should be equipped with an automatic interlocking protection system for the sterile production environment. When the sterile production environment is damaged, the system should immediately alarm and automatically enter the relevant processing flow according to the degree of damage. 5.8 The clean room space and equipment surface should not have colony growth at all control points after bacterial culture test, SE ≥ 5. 5.9 After sterilization, the packaging material is tested for microorganisms, and the results show that there should be no colony growth, SE ≥ 5. 5.10 Under normal filling production conditions, the residual concentration of hydrogen peroxide in the packaged finished product should not exceed 0.5 mg/L. 5.11 The temperature regulator of the sterile machine should stably and reliably control the temperature of the heat-sealed part, should be adjustable within a certain range, and should be equipped with a heating indicator. The temperature difference on the effective heat-sealed length of the heat-sealed part surface should be within ± 10 °C 5.12 The filling accuracy of the sterile machine should comply with the provisions of Table 1, and the average actual content should comply with the provisions of JJF1070. Table 1 Filling accuracy
Net content (
Filling accuracy/%
The appearance of the opening should be flat, with clear mesh, no wrinkles, burning and jade penetration. 5.13 Packaging bag sealing
5.14 The heat 0
of the packaging bag shall be within the values listed in Table 2.
The strength (the tensile force that the heat seal can withstand) should not be less than the
material described in the table.
Thickness refers to the thickness of the heat sealing layer material. The material of the heat sealing part is mostly PE or PP that is easy to heat seal. Table 2 Heat sealing strength
Material Kang degree (expressed by "R\)/mm
Heat sealing strength/(N15ml)
5.15 The aseptic machine is positioned by color code, and the cutting position error shall not exceed ±2mm. When other forms are used to control the length of the bag, when the bag length is less than 100mm, the error shall not exceed 9±2mm; when the bag length is greater than or equal to 100mm, the error shall not exceed ±2% of the bag length. After filling, the packaged parts shall be subjected to static pressure and skin fall tests, and the seals shall be intact. 5.16
Under normal UHT conditions, the sterility qualification rate of the packaged products shall not be less than 99.9%. 5.17
The qualified rate of packages shall not be less than 99%.
The noise sound pressure level of the sterile machine shall not be greater than 75dB(A). 5.20
The insulation resistance measured when 500Vd.c. is applied between the power circuit wire and the protective grounding circuit shall not be less than 1Mα. 5.21 The sterile machine shall have a reliable grounding device and an obvious grounding mark. The ground resistance shall comply with the requirements of 19.2 in GB5226.1-2002.
5.22 All circuit conductors of electrical equipment and the protective grounding circuit shall be subjected to a withstand voltage test of at least 1s. 5.23 The materials and components of the aseptic machine shall comply with the following provisions. 5.23.1 When the filling material is food, the safety and sanitation requirements of the material selection, design, manufacturing and configuration principles of the aseptic machine shall comply with the provisions of GB16798. When the filling material is medicine, the surface material of the aseptic machine in contact with the filling material and packaging material shall comply with the relevant national regulations on pharmaceutical production equipment.
http://foodmate.net5.23.2 The mechanical design hygiene and safety of the aseptic machine shall comply with the requirements of GB19891. GB/T2 4570—2009
5.23.3 The surface of equipment that contacts packaging materials and filling materials should be smooth, flat, easy to clean or disinfect, corrosion-resistant, and should not react chemically with filling materials.
5.23.4 The surfaces of containers, pipes, valves, etc. that contact filling materials or require CIP cleaning should be polished, without dead angles, welds should be polished, and there should be no gaps for material storage. The contact area of the aseptic machine filling materials should not contaminate the materials. The surface roughness Ra value of containers and valves should not exceed 1.6μm, and the roughness Ra value of non-product contact surface parts in the clean area (room) should not exceed 3.2μm. 5.23.5 The purchased valves, detection components and pipe fittings that contact filling materials, sterile water and sterile gas should be of aseptic type or structural type without cleaning dead angles.
5.23.6 Lubricants and coolants used in the equipment should not contaminate the filling materials or containers. 5.23.7 Rubber parts and seals in the sterile machine that are in contact with (or may be in contact with) disinfectants or cleaning fluids should be resistant to oxidation and corrosion, such as fluororubber, silicone rubber, EPDM rubber, etc. 5.23.8 The raw materials and purchased parts used in the sterile machine should have a quality certificate from the manufacturer. If there is no quality certificate, they should be accepted according to the relevant product standards before they can be put into use. 5.24 The safety protection of the sterile machine shall comply with the following provisions: a) The safety protection of the sterile machine shall comply with the provisions of JB7233 b) The sterile machine/has clear and eye-catching safety warning signs such as operation, lubrication, anti-scalding and anti-chemical injury. Safety signs shall comply with the provisions of GB2894GB16179 and GB/T1
16273.1
c) When opening the protective device of the sterile machine may cause danger, the sterile machine shall be equipped with interlock protection. The device shall be interlocked with the mechanical transmission mechanism of the sterile machine. When the packaging material or filling material is below the control lower limit or there is no material, the pipe or alarm shall be reported and the machine shall be shut down; d) All parts and fasteners such as bolts and nuts of the sterile machine shall be fixed reliably and shall not be loose or fall off due to vibration; e) Rubber parts and plastic parts (such as sealing gaskets and plastic frames that need to be fixed) bonded on the contact surface of the filling material shall be continuously bonded to ensure that they do not fall off under normal working conditions (cleaning, heating, pressurization); D) Protective covers shall be set when the moving parts such as gears, belts, chains, friction wheels of the sterile machine are exposed. The reciprocating motion of the machine should have a protective device at the extreme position:
g) The power switch, start and stop buttons of the sterile machine should be flexible and reliable, h) When the sterile machine uses volatile sterilizing liquid, the storage box or immersion box should be closed and have a safe protective capacity. 5.25 The appearance quality of the sterile machine should meet the following requirements. 5.25.1 The paint and spray coating of the non-processed surface should be flat and smooth, with uniform color, and should not have obvious scratches, dirt, flow marks, bubbles and other defects.
5.25.2 The surface-treated parts should have uniform color and grooves, without bubbles, delamination, rust and other defects. 5.26 The hydrogen peroxide content in the sterile machine operating environment should not exceed 2mg/L6 Test method
6.1 Test conditions
6.1.1 The test environment temperature should be 18℃～28℃. 6.1.2 The packaging materials used in the test shall comply with the provisions of 4.3.5 and GB19741, and the filling materials shall be liquid media (such as juice, etc.) that comply with national and industry standards. 6.1.3 The cleanliness of the clean area (room) shall be measured according to the methods specified in GB/T16292, GB/T16293 and GB/T16294, and shall comply with the provisions of 5.6 [the cleanliness of the sterile clean room (area) shall meet the requirements before the tests of 6.2 to 6.14 can be carried out]. 6.2 Idle running test
After each sterile machine is assembled, an idle running test shall be carried out. The continuous idle running time at the rated speed shall not be less than 6 hours. The machine performance shall be checked and shall comply with the provisions of 5.2 and 5.3. 5
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GB/T24570—2009
6.3 Inspection of the sealing of the gas circuit, pipeline and lubrication system 6.3.1 Visually observe whether there is steam leakage and dripping at the steam pipe seal, which shall comply with the provisions of 5.4. 6.3.2 Apply soapy water or detergent water to the seal of the pneumatic component seal and observe whether there is air leakage. It should comply with the provisions of 5.4. 6.3.3 Use absorbent cotton to gently wipe around the seal of the lubrication system and observe whether there is oil stain on the absorbent cotton. It should comply with the provisions of 5.4. 6.3.4 Use absorbent cotton to gently wipe around the seal of the conveying pipeline and observe whether there is material on the absorbent cotton. It should comply with the provisions of 5.4. 6.4 Production capacity test
After the aseptic machine is in normal operation, continue to package for 0.5h, count the number of packages, and calculate the production capacity according to formula (1). It should comply with the provisions of 5.5. V=
Where:
V—production capacity, the unit is bags per hour (bag/h); M—the number of completed packages, the unit is.
6.5 Microbiological validation test
6.5.1 Colony test on clean room space and its equipment surfaces.....(1)
Colony test on clean room space: First, place the plate filled with culture medium (sterilized) into the clean area (room) (whose cleanliness has reached the a)
100 grade standard). After cleaning and sterilization according to SOP, open the plate at the set key point for no more than 10 minutes, then operate the sterilizing machine normally, maintain air flow in the clean area (room), and conduct dynamic testing. , after 30 minutes, cover with blood, and then put it in the incubator for cultivation. Test according to the provisions of GB/T4789.2, observe the results, and it should meet the requirements of 5.8; b) Clean room equipment surface colony test: smear test on the surface of clean room equipment, use sterile cotton swab to smear and sample the designated position (generally arranged on the surface of equipment that is not easy to clean, and the position with extremely high sterility requirements, such as near the filling head), test according to the provisions of GB/T4789.2, observe the results, and it should meet the requirements of 5.8. 6.5.2 Microbiological verification test of packaging materials Take 20 empty bags after sterilization and sealing, cut the test bags along the longitudinal seam in the sterile laboratory, cut them into the largest rectangular shape, and measure the area, accurate to 0.1cm2. Take 100mL of sterile water, wipe the surface to be tested repeatedly with sterile cotton soaked in sterile water, and test the total number of bacteria according to the provisions of GB/T4789.2. The result should meet the requirements of 5.9. 6.6 Hydrogen peroxide residue test
The residual amount of hydrogen peroxide shall be determined according to the method of "Technical Specifications for Disinfection" (2002 Edition), and the determination results shall comply with the provisions of 5.10. 6.7 Temperature control test
Adjust the temperature regulator to the heat sealing temperature value, and use a thermometer (the accuracy of the thermometer is ±1.5℃ and the resolution is 0.1℃) to measure three points on the effective length of the heat sealing part, one of which is the midpoint, and the other two are respectively taken at 15mm from both ends of the effective heat sealing length. The temperature difference of the three points measured shall comply with the provisions of 5.11.
6.8 Filling accuracy test
Use a calibration scale with a maximum allowable error less than or equal to one-third of the allowable deviation of the net content of the package being tested to weigh the net content of the filling material according to the provisions of Table 3. The difference between the measured net content of the filling material and the marked net content shall comply with the provisions of 5.12. Table 3 Sampling plan for metrological inspection
Number of sampling pieces
Batch of packaged items N
Correction value of average actual content (Λ·S)
Correction factor
Number of pieces allowed to exceed the filling
actual content standard deviation precision by 1 times or S
equal to 2 times
Number of pieces allowed to exceed
2 times the filling precision
Batch of packaged items N
100～500
501~3200
Greater than 3200
Number of sampling pieces
Note 1: The confidence level of this sampling plan is 998%. Table 3 (continued)
Correction value of average actual content (A·S)
Correction factor
GB/T24570—2009
Number of pieces allowed to exceed the filling accuracy by 1 times or
Number of pieces equal to 2 times the standard deviation of actual content
Number of pieces allowed to exceed the filling accuracy by 2 times
Note 2: When the batch size of an inspection lot is less than or equal to 10 pieces, only the actual content of each single piece of quantitatively packaged commodity shall be inspected and evaluated, and the average actual content shall not be calculated
-(2)
Where:
- The average actual content of the sampled packages: - measured net content of the filled material
- sampling
The average actual content meets the requirements of formula (3):
Wherein:
- standard net content;
=to.99s×
Correction factor
- actual food safety standard deviation,
Note: The average actual content should be
6.9 Sterility pass rate test
4 (Q)
days or equal to the marked net content minus the average actual content correction value S.
(3)
From each filling head, 2400 bags of finished packaging are drawn. The drawing method is: one bag is drawn from every 5 bags. Place the finished bags in a constant temperature of 38℃ for 5 days, test the pH value of the filling material, compare it with the pH value of the original filling material, and count the number of pH difference greater than 0.2 P, and the number of swollen bags P3
Calculation is shown in formula (4):
Sterile qualified rate III
Where:
Pr——the number of pH difference greater than 0.2, in bags; Pa
The number of swollen bags, in bags.
x1000%
The calculation result should comply with the provisions of 5.17. After three consecutive batches are qualified, it is determined that the packaged product meets the sterility requirements. 6.10 Package qualified rate test
6.10.1 Package appearance quality test
·(4)
After the sterilizer has been working normally, 100 bags of samples are drawn three times at rated speed, and the interval between each drawing is not less than 1 minute. Visually inspect the appearance quality of the sample bags and measure the photoelectric tracking cutting position error. It should meet the requirements of 5.13 and 5.15, and count the number of unqualified products.
http://foodmate.netGB/T24570—2009
6.10.2 Heat seal strength test
Take 25 bags of samples with qualified appearance quality, and extract samples from the seal of each bag according to the method in Table 4. Each sample is 15mm wide, 50mm long in the direction perpendicular to the seal length, and 100mm long after being flattened at 180°. Place the two ends of the sample with the seal in the middle in the fixture of the electronic universal testing machine. The distance between the fixtures is 50mm, the test speed is 300mm/min±20mm/min, read the maximum load when the sample breaks, and take the lowest value of the sample load for each bag as the sealing strength of the bag. It should comply with the provisions of 5.14, and count the number of unqualified products. 4 Sampling plan for heat sealing strength test
Total length of bag seal (L)/mm
Location of sampling points
and number
6.10.3 Static pressure and drop test
15mm≤L≤30mm
Take a sample from the middle part of the bag seal
30mm1 Visually observe whether there is steam leakage and dripping at the steam pipe seal, which shall comply with the provisions of 5.4. 6.3.2 Apply soapy water or detergent water to the seal of the pneumatic component seal and observe whether there is air leakage, which shall comply with the provisions of 5.4. 6.3.3 Gently wipe the seal of the lubrication system with absorbent cotton and observe whether there is oil stain on the absorbent cotton, which shall comply with the provisions of 5.4. 6.3.4 Gently wipe the seal of the conveying pipeline with absorbent cotton and observe whether there is material on the absorbent cotton, which shall comply with the provisions of 5.4. 6.4 Production capacity test
After the aseptic machine is in normal operation, it will continuously package for 0.5h, count the number of packages, and calculate the production capacity according to formula (1), which shall comply with the provisions of 5.5. V=
Where:
V—production capacity, in bags per hour (bag/h); M—number of completed packages, in units.
6.5 Microbiological validation test
6.5.1 Colony test on clean room space and its equipment surfaces.....(1)
Colony test on clean room space: First, place the plate filled with culture medium (sterilized) into the clean area (room) (whose cleanliness has reached the a)
100 grade standard). After cleaning and sterilization according to SOP, open the plate at the set key point for no more than 10 minutes, then operate the sterilizing machine normally, maintain air flow in the clean area (room), and conduct dynamic testing. , after 30 minutes, cover with blood, and then put it in the incubator for cultivation. Test according to the provisions of GB/T4789.2, observe the results, and it should meet the requirements of 5.8; b) Clean room equipment surface colony test: smear test on the surface of clean room equipment, use sterile cotton swab to smear and sample the designated position (generally arranged on the surface of equipment that is not easy to clean, and the position with extremely high sterility requirements, such as near the filling head), test according to the provisions of GB/T4789.2, observe the results, and it should meet the requirements of 5.8. 6.5.2 Microbiological verification test of packaging materials Take 20 empty bags after sterilization and sealing, cut the test bags along the longitudinal seam in the sterile laboratory, cut them into the largest rectangular shape, and measure the area, accurate to 0.1cm2. Take 100mL of sterile water, wipe the surface to be tested repeatedly with sterile cotton soaked in sterile water, and test the total number of bacteria according to the provisions of GB/T4789.2. The result should meet the requirements of 5.9. 6.6 Hydrogen peroxide residue test
The residual amount of hydrogen peroxide shall be determined according to the method of "Technical Specifications for Disinfection" (2002 Edition), and the determination results shall comply with the provisions of 5.10. 6.7 Temperature control test
Adjust the temperature regulator to the heat sealing temperature value, and use a thermometer (the accuracy of the thermometer is ±1.5℃ and the resolution is 0.1℃) to measure three points on the effective length of the heat sealing part, one of which is the midpoint, and the other two are respectively taken at 15mm from both ends of the effective heat sealing length. The temperature difference of the three points measured shall comply with the provisions of 5.11.
6.8 Filling accuracy test
Use a calibration scale with a maximum allowable error less than or equal to one-third of the allowable deviation of the net content of the package being tested to weigh the net content of the filling material according to the provisions of Table 3. The difference between the measured net content of the filling material and the marked net content shall comply with the provisions of 5.12. Table 3 Sampling plan for metrological inspection
Number of sampling pieces
Batch of packaged items N
Correction value of average actual content (Λ·S)
Correction factor
Number of pieces allowed to exceed the filling
actual content standard deviation precision by 1 times or S
equal to 2 times
Number of pieces allowed to exceed
2 times the filling precision
Batch of packaged items N
100～500
501~3200
Greater than 3200
Number of sampling pieces
Note 1: The confidence level of this sampling plan is 998%. Table 3 (continued)
Correction value of average actual content (A·S)
Correction factor
GB/T24570—2009
Number of pieces allowed to exceed the filling accuracy by 1 times or
Number of pieces equal to 2 times the standard deviation of actual content
Number of pieces allowed to exceed the filling accuracy by 2 times
Note 2: When the batch size of an inspection lot is less than or equal to 10 pieces, only the actual content of each single piece of quantitatively packaged commodity shall be inspected and evaluated, and the average actual content shall not be calculated
-(2)
Where:
- The average actual content of the sampled packages: - measured net content of the filled material
- sampling
The average actual content meets the requirements of formula (3):
Wherein:
- standard net content;
=to.99s×
Correction factor
- actual food safety standard deviation,
Note: The average actual content should be
6.9 Sterility pass rate test
4 (Q)
days or equal to the marked net content minus the average actual content correction value S.
(3)
From each filling head, 2400 bags of finished packaging are drawn. The drawing method is: one bag is drawn from every 5 bags. Place the finished bags in a constant temperature of 38℃ for 5 days, test the pH value of the filling material, compare it with the pH value of the original filling material, and count the number of pH difference greater than 0.2 P, and the number of swollen bags P3
Calculation is shown in formula (4):
Sterile qualified rate III
Where:
Pr——the number of pH difference greater than 0.2, in bags; Pa
The number of swollen bags, in bags.
x1000%
The calculation result should comply with the provisions of 5.17. After three consecutive batches are qualified, it is determined that the packaged product meets the sterility requirements. 6.10 Package qualified rate test
6.10.1 Package appearance quality test
·(4)
After the sterilizer has been working normally, 100 bags of samples are drawn three times at rated speed, and the interval between each drawing is not less than 1 minute. Visually inspect the appearance quality of the sample bags and measure the photoelectric tracking cutting position error. It should meet the requirements of 5.13 and 5.15, and count the number of unqualified products.
http://foodmate.netGB/T24570—2009
6.10.2 Heat seal strength test
Take 25 bags of samples with qualified appearance quality, and extract samples from the seal of each bag according to the method in Table 4. Each sample is 15mm wide, 50mm long in the direction perpendicular to the seal length, and 100mm long after being flattened at 180°. Place the two ends of the sample with the seal in the middle in the fixture of the electronic universal testing machine. The distance between the fixtures is 50mm, the test speed is 300mm/min±20mm/min, read the maximum load when the sample breaks, and take the lowest value of the sample load for each bag as the sealing strength of the bag. It should comply with the provisions of 5.14, and count the number of unqualified products. 4 Sampling plan for heat sealing strength test
Total length of bag seal (L)/mm
Location of sampling points
and number
6.10.3 Static pressure and drop test
15mm≤L≤30mm
Take a sample from the middle part of the bag seal
30mm1 Visually observe whether there is steam leakage and dripping at the steam pipe seal, which shall comply with the provisions of 5.4. 6.3.2 Apply soapy water or detergent water to the seal of the pneumatic component seal and observe whether there is air leakage, which shall comply with the provisions of 5.4. 6.3.3 Gently wipe the seal of the lubrication system with absorbent cotton and observe whether there is oil stain on the absorbent cotton, which shall comply with the provisions of 5.4. 6.3.4 Gently wipe the seal of the conveying pipeline with absorbent cotton and observe whether there is material on the absorbent cotton, which shall comply with the provisions of 5.4. 6.4 Production capacity test
After the aseptic machine is in normal operation, it will continuously package for 0.5h, count the number of packages, and calculate the production capacity according to formula (1), which shall comply with the provisions of 5.5. V=
Where:
V—production capacity, in bags per hour (bag/h); M—number of completed packages, in units.
6.5 Microbiological validation test
6.5.1 Colony test on clean room space and its equipment surfaces.....(1)
Colony test on clean room space: First, place the plate filled with culture medium (sterilized) into the clean area (room) (whose cleanliness has reached the a)
100 grade standard). After cleaning and sterilization according to SOP, open the plate at the set key point for no more than 10 minutes, then operate the sterilizing machine normally, maintain air flow in the clean area (room), and conduct dynamic testing. , after 30 minutes, cover with blood, and then put it in the incubator for cultivation. Test according to the provisions of GB/T4789.2, observe the results, and it should meet the requirements of 5.8; b) Clean room equipment surface colony test: smear test on the surface of clean room equipment, use sterile cotton swab to smear and sample the designated position (generally arranged on the surface of equipment that is not easy to clean, and the position with extremely high sterility requirements, such as near the filling head), test according to the provisions of GB/T4789.2, observe the results, and it should meet the requirements of 5.8. 6.5.2 Microbiological verification test of packaging materials Take 20 empty bags after sterilization and sealing, cut the test bags along the longitudinal seam in the sterile laboratory, cut them into the largest rectangular shape, and measure the area, accurate to 0.1cm2. Take 100mL of sterile water, wipe the surface to be tested repeatedly with sterile cotton soaked in sterile water, and test the total number of bacteria according to the provisions of GB/T4789.2. The result should meet the requirements of 5.9. 6.6 Hydrogen peroxide residue test
The residual amount of hydrogen peroxide shall be determined according to the method of "Technical Specifications for Disinfection" (2002 Edition), and the determination results shall comply with the provisions of 5.10. 6.7 Temperature control test
Adjust the temperature regulator to the heat sealing temperature value, and use a thermometer (the accuracy of the thermometer is ±1.5℃ and the resolution is 0.1℃) to measure three points on the effective length of the heat sealing part, one of which is the midpoint, and the other two are respectively taken at 15mm from both ends of the effective heat sealing length. The temperature difference of the three points measured shall comply with the provisions of 5.11.
6.8 Filling accuracy test
Use a calibration scale with a maximum allowable error less than or equal to one-third of the allowable deviation of the net content of the package being tested to weigh the net content of the filling material according to the provisions of Table 3. The difference between the measured net content of the filling material and the marked net content shall comply with the provisions of 5.12. Table 3 Sampling plan for metrological inspection
Number of sampling pieces
Batch of packaged items N
Correction value of average actual content (Λ·S)
Correction factor
Number of pieces allowed to exceed the filling
actual content standard deviation precision by 1 times or Swww.bzxz.net
equal to 2 times
Number of pieces allowed to exceed
2 times the filling precision
Batch of packaged items N
100～500
501~3200
Greater than 3200
Number of sampling pieces
Note 1: The confidence level of this sampling plan is 998%. Table 3 (continued)
Correction value of average actual content (A·S)
Correction factor
GB/T24570—2009
Number of pieces allowed to exceed the filling accuracy by 1 times or
Number of pieces equal to 2 times the standard deviation of actual content
Number of pieces allowed to exceed the filling accuracy by 2 times
Note 2: When the batch size of an inspection lot is less than or equal to 10 pieces, only the actual content of each single piece of quantitatively packaged commodity shall be inspected and evaluated, and the average actual content shall not be calculated
-(2)
Where:
- The average actual content of the sampled packages: - measured net content of the filled material
- sampling
The average actual content meets the requirements of formula (3):
Wherein:
- standard net content;
=to.99s×
Correction factor
- actual food safety standard deviation,
Note: The average actual content should be
6.9 Sterility pass rate test
4 (Q)
days or equal to the marked net content minus the average actual content correction value S.
(3)
From each filling head, 2400 bags of finished packaging are drawn. The drawing method is: one bag is drawn from every 5 bags. Place the finished bags in a constant temperature of 38℃ for 5 days, test the pH value of the filling material, compare it with the pH value of the original filling material, and count the number of pH difference greater than 0.2 P, and the number of swollen bags P3
Calculation is shown in formula (4):
Sterile qualified rate III
Where:
Pr——the number of pH difference greater than 0.2, in bags; Pa
The number of swollen bags, in bags.
x1000%
The calculation result should comply with the provisions of 5.17. After three consecutive batches are qualified, it is determined that the packaged product meets the sterility requirements. 6.10 Package qualified rate test
6.10.1 Package appearance quality test
·(4)
After the sterilizer has been working normally, 100 bags of samples are drawn three times at rated speed, and the interval between each drawing is not less than 1 minute. Visually inspect the appearance quality of the sample bags and measure the photoelectric tracking cutting position error. It should meet the requirements of 5.13 and 5.15, and count the number of unqualified products.
http://foodmate.netGB/T24570—2009
6.10.2 Heat seal strength test
Take 25 bags of samples with qualified appearance quality, and extract samples from the seal of each bag according to the method in Table 4. Each sample is 15mm wide, 50mm long in the direction perpendicular to the seal length, and 100mm long after being flattened at 180°. Place the two ends of the sample with the seal in the middle in the fixture of the electronic universal testing machine. The distance between the fixtures is 50mm, the test speed is 300mm/min±20mm/min, read the maximum load when the sample breaks, and take the lowest value of the sample load for each bag as the sealing strength of the bag. It should comply with the provisions of 5.14, and count the number of unqualified products. 4 Sampling plan for heat sealing strength test
Total length of bag seal (L)/mm
Location of sampling points
and number
6.10.3 Static pressure and drop test
15mm≤L≤30mm
Take a sample from the middle part of the bag seal
30mm8 requirements; b) Clean room equipment surface colony test: smear test on the surface of clean room equipment, use sterile cotton swab to smear and sample the designated position (generally arranged on the surface of equipment that is not easy to clean, and the position with extremely high sterility requirements, such as near the filling head), test according to the provisions of GB/T4789.2, observe the results, and it should meet the requirements of 5.8. 6.5.2 Microbiological verification test of packaging materials Take 20 empty bags after sterilization and sealing, cut the test bags along the longitudinal seam in the sterile laboratory, cut them into the largest rectangular shape, and measure the area with an accuracy of 0.1cm2. Take 100mL of sterile water, wipe the surface to be tested repeatedly with sterile cotton soaked in sterile water, and test the total number of bacteria according to the provisions of GB/T4789.2. The result should meet the requirements of 5.9. 6.6 Hydrogen peroxide residue test
The residual amount of hydrogen peroxide is determined according to the method of "Disinfection Technical Specifications" (2002 edition), and the determination results meet the requirements of 5.10. 6.7 Temperature Control Test
Adjust the temperature regulator to the heat seal temperature value, and use a thermometer (temperature meter accuracy is ±1.5℃, resolution is 0.1℃) to measure three points on the effective length of the heat seal part, one of which is the midpoint, and the other two are respectively taken at 15mm from both ends of the effective heat seal length. The temperature difference of the three points measured shall comply with the provisions of 5.11.
6.8 Filling Accuracy Test
Use a calibration scale with a maximum allowable error less than or equal to one-third of the allowable deviation of the net content of the package being tested to weigh the net content of the filling material according to the provisions of Table 3. The difference between the measured net content of the filling material and the marked net content shall comply with the provisions of 5.12. Table 3 Sampling plan for metrological inspection
Number of sampling pieces
Batch of packaged items N
Correction value of average actual content (Λ·S)
Correction factor
Number of pieces allowed to exceed the filling
actual content standard deviation precision by 1 times or S
equal to 2 times
Number of pieces allowed to exceed
2 times the filling precision
Batch of packaged items N
100～500
501~3200
Greater than 3200
Number of sampling pieces
Note 1: The confidence level of this sampling plan is 998%. Table 3 (continued)
Correction value of average actual content (A·S)
Correction factor
GB/T24570—2009
Number of pieces allowed to exceed the filling accuracy by 1 times or
Number of pieces equal to 2 times the standard deviation of actual content
Number of pieces allowed to exceed the filling accuracy by 2 times
Note 2: When the batch size of an inspection lot is less than or equal to 10 pieces, only the actual content of each single piece of quantitatively packaged commodity shall be inspected and evaluated, and the average actual content shall not be calculated
-(2)
Where:
- The average actual content of the sampled packages: - measured net content of the filled material
- sampling
The average actual content meets the requirements of formula (3):
Wherein:
- standard net content;
=to.99s×
Correction factor
- actual food safety standard deviation,
Note: The average actual content should be
6.9 Sterility pass rate test
4 (Q)
days or equal to the marked net content minus the average actual content correction value S.
(3)
From each filling head, 2400 bags of finished packaging are drawn. The drawing method is: one bag is drawn from every 5 bags. Place the finished bags in a constant temperature of 38℃ for 5 days, test the pH value of the filling material, compare it with the pH value of the original filling material, and count the number of pH difference greater than 0.2 P, and the number of swollen bags P3
Calculation is shown in formula (4):
Sterile qualified rate III
Where:
Pr——the number of pH difference greater than 0.2, in bags; Pa
The number of swollen bags, in bags.
x1000%
The calculation result should comply with the provisions of 5.17. After three consecutive batches are qualified, it is determined that the packaged product meets the sterility requirements. 6.10 Package qualified rate test
6.10.1 Package appearance quality test
·(4)
After the sterilizer has been working normally, 100 bags of samples are drawn three times at rated speed, and the interval between each drawing is not less than 1 minute. Visually inspect the appearance quality of the sample bags and measure the photoelectric tracking cutting position error. It should meet the requirements of 5.13 and 5.15, and count the number of unqualified products.
http://foodmate.netGB/T24570—2009
6.10.2 Heat seal strength test
Take 25 bags of samples with qualified appearance quality, and extract samples from the seal of each bag according to the method in Table 4. Each sample is 15mm wide, 50mm long in the direction perpendicular to the seal length, and 100mm long after being flattened at 180°. Place the two ends of the sample with the seal in the middle in the fixture of the electronic universal testing machine. The distance between the fixtures is 50mm, the test speed is 300mm/min±20mm/min, read the maximum load when the sample breaks, and take the lowest value of the sample load for each bag as the sealing strength of the bag. It should comply with the provisions of 5.14, and count the number of unqualified products. 4 Sampling plan for heat sealing strength test
Total length of bag seal (L)/mm
Location of sampling points
and number
6.10.3 Static pressure and drop test
15mm≤L≤30mm
Take a sample from the middle part of the bag seal
30mm8 requirements; b) Clean room equipment surface colony test: smear test on the surface of clean room equipment, use sterile cotton swab to smear and sample the designated position (generally arranged on the surface of equipment that is not easy to clean, and the position with extremely high sterility requirements, such as near the filling head), test according to the provisions of GB/T4789.2, observe the results, and it should meet the requirements of 5.8. 6.5.2 Microbiological verification test of packaging materials Take 20 empty bags after sterilization and sealing, cut the test bags along the longitudinal seam in the sterile laboratory, cut them into the largest rectangular shape, and measure the area with an accuracy of 0.1cm2. Take 100mL of sterile water, wipe the surface to be tested repeatedly with sterile cotton soaked in sterile water, and test the total number of bacteria according to the provisions of GB/T4789.2. The result should meet the requirements of 5.9. 6.6 Hydrogen peroxide residue test
The residual amount of hydrogen peroxide is determined according to the method of "Disinfection Technical Specifications" (2002 edition), and the determination results meet the requirements of 5.10. 6.7 Temperature Control Test
Adjust the temperature regulator to the heat seal temperature value, and use a thermometer (temperature meter accuracy is ±1.5℃, resolution is 0.1℃) to measure three points on the effective length of the heat seal part, one of which is the midpoint, and the other two are respectively taken at 15mm from both ends of the effective heat seal length. The temperature difference of the three points measured shall comply with the provisions of 5.11.
6.8 Filling Accuracy Test
Use a calibration scale with a maximum allowable error less than or equal to one-third of the allowable deviation of the net content of the package being tested to weigh the net content of the filling material according to the provisions of Table 3. The difference between the measured net content of the filling material and the marked net content shall comply with the provisions of 5.12. Table 3 Sampling plan for metrological inspection
Number of sampling pieces
Batch of packaged items N
Correction value of average actual content (Λ·S)
Correction factor
Number of pieces allowed to exceed the filling
actual content standard deviation precision by 1 times or S
equal to 2 times
Number of pieces allowed to exceed
2 times the filling precision
Batch of packaged items N
100～500
501~3200
Greater than 3200
Number of sampling pieces
Note 1: The confidence level of this sampling plan is 998%. Table 3 (continued)
Correction value of average actual content (A·S)
Correction factor
GB/T24570—2009
Number of pieces allowed to exceed the filling accuracy by 1 times or
Number of pieces equal to 2 times the standard deviation of actual content
Number of pieces allowed to exceed the filling accuracy by 2 times
Note 2: When the batch size of an inspection lot is less than or equal to 10 pieces, only the actual content of each single piece of quantitatively packaged commodity shall be inspected and evaluated, and the average actual content shall not be calculated
-(2)
Where:
- The average actual content of the sampled packages: - measured net content of the filled material
- sampling
The average actual content meets the requirements of formula (3):
Wherein:
- standard net content;
=to.99s×
Correction factor
- actual food safety standard deviation,
Note: The average actual content should be
6.9 Sterility pass rate test
4 (Q)
days or equal to the marked net content minus the average actual content correction value S.
(3)
From each filling head, 2400 bags of finished packaging are drawn. The drawing method is: one bag is drawn from every 5 bags. Place the finished bags in a constant temperature of 38℃ for 5 days, test the pH value of the filling material, compare it with the pH value of the original filling material, and count the number of pH difference greater than 0.2 P, and the number of swollen bags P3
Calculation is shown in formula (4):
Sterile qualified rate III
Where:
Pr——the number of pH difference greater than 0.2, in bags; Pa
The number of swollen bags, in bags.
x1000%
The calculation result should comply with the provisions of 5.17. After three consecutive batches are qualified, it is determined that the packaged product meets the sterility requirements. 6.10 Package qualified rate test
6.10.1 Package appearance quality test
·(4)
After the sterilizer has been working normally, 100 bags of samples are drawn three times at rated speed, and the interval between each drawing is not less than 1 minute. Visually inspect the appearance quality of the sample bags and measure the photoelectric tracking cutting position error. It should meet the requirements of 5.13 and 5.15, and count the number of unqualified products.
http://foodmate.netGB/T24570—2009
6.10.2 Heat seal strength test
Take 25 bags of samples with qualified appearance quality, and extract samples from the seal of each bag according to the method in Table 4. Each sample is 15mm wide, 50mm long in the direction perpendicular to the seal length, and 100mm long after being flattened at 180°. Place the two ends of the sample with the seal in the middle in the fixture of the electronic universal testing machine. The distance between the fixtures is 50mm, the test speed is 300mm/min±20mm/min, read the maximum load when the sample breaks, and take the lowest value of the sample load for each bag as the sealing strength of the bag. It should comply with the provisions of 5.14, and count the number of unqualified products. 4 Sampling plan for heat sealing strength test
Total length of bag seal (L)/mm
Location of sampling points
and number
6.10.3 Static pressure and drop test
15mm≤L≤30mm
Take a sample from the middle part of the bag seal
30mm12. Table 3 Sampling plan for metrological inspection
Number of sampling pieces
Batch of package N
Correction value of average actual content (Λ·S)
Correction factor
Number of pieces allowed to exceed the filling
actual content standard deviation precision by 1 times or S
equal to 2 times
Number of pieces allowed to exceed the filling precision
2 times
Batch of package N
100～500
501~3200
Greater than 3200
Number of sampling pieces
Note 1: The confidence level of this sampling plan is 998%. Table 3 (continued)
Correction value of average actual content (A·S)
Correction factor
GB/T24570—2009
Number of pieces allowed to exceed the filling accuracy by 1 times or
Number of pieces equal to 2 times the standard deviation of actual content
Number of pieces allowed to exceed the filling accuracy by 2 times
Note 2: When the batch size of an inspection lot is less than or equal to 10 pieces, only the actual content of each single piece of quantitatively packaged commodity shall be inspected and evaluated, and the average actual content shall not be calculated
-(2)
Where:
- The average actual content of the sampled packages: - measured net content of the filled material
- sampling
The average actual content meets the requirements of formula (3):
Wherein:
- standard net content;
=to.99s×
Correction factor
- actual food safety standard deviation,
Note: The average actual content should be
6.9 Sterility pass rate test
4 (Q)
days or equal to the marked net content minus the average actual content correction value S.
(3)
From each filling head, 2400 bags of finished packaging are drawn. The drawing method is: one bag is drawn from every 5 bags. Place the finished bags in a constant temperature of 38℃ for 5 days, test the pH value of the filling material, compare it with the pH value of the original filling material, and count the number of pH difference greater than 0.2 P, and the number of swollen bags P3
Calculation is shown in formula (4):
Sterile qualified rate III
Where:
Pr——the number of pH difference greater than 0.2, in bags; Pa
The number of swollen bags, in bags.
x1000%
The calculation result should comply with the provisions of 5.17. After three consecutive batches are qualified, it is determined that the packaged product meets the sterility requirements. 6.10 Package qualified rate test
6.10.1 Package appearance quality test
·(4)
After the sterilizer has been working normally, 100 bags of samples are drawn three times at rated speed, and the interval between each drawing is not less than 1 minute. Visually inspect the appearance quality of the sample bags and measure the photoelectric tracking cutting position error. It should meet the requirements of 5.13 and 5.15, and count the number of unqualified products.
http://foodmate.netGB/T24570—2009
6.10.2 Heat seal strength test
Take 25 bags of samples with qualified appearance quality, and extract samples from the seal of each bag according to the method in Table 4. Each sample is 15mm wide, 50mm long in the direction perpendicular to the seal length, and 100mm long after being flattened at 180°. Place the two ends of the sample with the seal in the middle in the fixture of the electronic universal testing machine. The distance between the fixtures is 50mm, the test speed is 300mm/min±20mm/min, read the maximum load when the sample breaks, and take the lowest value of the sample load for each bag as the sealing strength of the bag. It should comply with the provisions of 5.14, and count the number of unqualified products. 4 Sampling plan for heat sealing strength test
Total length of bag seal (L)/mm
Location of sampling points
and number
6.10.3 Static pressure and drop test
15mm≤L≤30mm
Take a sample from the middle part of the bag seal
30mm12. Table 3 Sampling plan for metrological inspection
Number of sampling pieces
Batch of package N
Correction value of average actual content (Λ·S)
Correction factor
Number of pieces allowed to exceed the filling
actual content standard deviation precision by 1 times or S
equal to 2 times
Number of pieces allowed to exceed the filling precision
2 times
Batch of package N
100～500
501~3200
Greater than 3200
Number of sampling pieces
Note 1: The confidence level of this sampling plan is 998%. Table 3 (continued)
Correction value of average actual content (A·S)
Correction factor
GB/T24570—2009
Number of pieces allowed to exceed the filling accuracy by 1 times or
Number of pieces equal to 2 times the standard deviation of actual content
Number of pieces allowed to exceed the filling accuracy by 2 times
Note 2: When the batch size of an inspection lot is less than or equal to 10 pieces, only the actual content of each single piece of quantitatively packaged commodity shall be inspected and evaluated, and the average actual content shall not be calculated
-(2)
Where:
- The average actual content of the sampled packages: - measured net content of the filled material
- sampling
The average actual content meets the requirements of formula (3):
Wherein:
- standard net content;
=to.99s×
Correction factor
- actual food safety standard deviation,
Note: The average actual content should be
6.9 Sterility pass rate test
4 (Q)
days or equal to the marked net content minus the average actual content correction value S.
(3)
From each filling head, 2400 bags of finished packaging are drawn. The drawing method is: one bag is drawn from every 5 bags. Place the finished bags in a constant temperature of 38℃ for 5 days, test the pH value of the filling material, compare it with the pH value of the original filling material, and count the number of pH difference greater than 0.2 P, and the number of swollen bags P3
Calculation is shown in formula (4):
Sterile qualified rate III
Where:
Pr——the number of pH difference greater than 0.2, in bags; Pa
The number of swollen bags, in bags.
x1000%
The calculation result should comply with the provisions of 5.17. After three consecutive batches are qualified, it is determined that the packaged product meets the sterility requirements. 6.10 Package qualified rate test
6.10.1 Package appearance quality test
·(4)
After the sterilizer has been working normally, 100 bags of samples are drawn three times at rated speed, and the interval between each drawing is not less than 1 minute. Visually inspect the appearance quality of the sample bags and measure the photoelectric tracking cutting position error. It should meet the requirements of 5.13 and 5.15, and count the number of unqualified products.
http://foodmate.netGB/T24570—2009
6.10.2 Heat seal strength test
Take 25 bags of samples with qualified appearance quality, and extract samples from the seal of each bag according to the method in Table 4. Each sample is 15mm wide, 50mm long in the direction perpendicular to the seal length, and 100mm long after being flattened at 180°. Place the two ends of the sample with the seal in the middle in the fixture of the electronic universal testing machine. The distance between the fixtures is 50mm, the test speed is 300mm/min±20mm/min, read the maximum load when the sample breaks, and take the lowest value of the sample load for each bag as the sealing strength of the bag. It should comply with the provisions of 5.14, and count the number of unqualified products. 4 Sampling plan for heat sealing strength test
Total length of bag seal (L)/mm
Location of sampling points
and number
6.10.3 Static pressure and drop test
15mm≤L≤30mm
Take a sample from the middle part of the bag seal
30mm
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