Some standard content:
ICS37.100.20
Packaging Industry Standard of the People's Republic of China
BB/T0051—2009
Thermal transfer film for infusion soft bags
Hot stamping foil for infusion bag2009-11-17Promulgated
2010-04-01Implementation
The Ministry of Industry and Information Technology of the People's Republic of ChinaPromulgated Announcement of the Ministry of Industry and Information Technology of the People's Republic of China
Engineering [2009] No. 63
The Ministry of Industry and Information Technology approved 139 industry standards including "Snowplow", including 29 automotive industry standards, 29 pharmaceutical equipment industry standards, 4 packaging industry standards, and 77 textile industry standards (see Appendix 1 for standard number, name, main content and starting implementation date): Approved the amendment to the textile industry standard FZ/T73001-2008 "Socks" (see Appendix 2), which is now announced and the standard amendment will be implemented from the date of announcement. The above standards for automobile, pharmaceutical equipment and packaging industries are published by China Planning Press, and the standards for textile industries are published by China Standards Press. Attachment: Numbers, names and starting dates of implementation of 4 packaging industry standards. Ministry of Industry and Information Technology of the People's Republic of China November 17, 2009
Attachment:
Numbers, names and starting dates of implementation of 4 packaging industry standards Standard number
BB/T0050—2009
BB/T0051-
BB/T0052—2009
BB/T0053—2009
Standard name
Hot coding ribbon
Thermal transfer film for infusion soft bags
Liquid milk co-extrusion packaging film and bag
In-mold Label
Starting date of implementation
2010-04-01
2010-04-01
2010-04-01
2010-04-01
Normative references
3 Terms and definitions
Inspection methods
Inspection rules
Marking, packaging, transportation and storage
BB/T00512009
BB/T0051—2009
This standard is proposed by the China Packaging Federation. Foreword
This standard is under the jurisdiction of the National Technical Committee for Packaging Standardization. The drafting units of this standard are: Jiaozuo Zhuoli Hot Stamping Materials Co., Ltd., Hangzhou Xingyong Composite Materials Co., Ltd., and China Packaging Research and Testing Center.
The main drafters of this standard are: Zhang Juhong, Zhang Zhenyu, Zhang Tielei, Niu Shumei, Geng Yanping, Deng Lixia, Wu Xiaoying. Ⅱ
1 Scope
Thermal transfer film for infusion soft bags
BB/T0051—2009
This standard specifies the product classification, requirements, inspection methods, inspection rules and marking, packaging, transportation and storage of thermal transfer film for infusion soft bags.
This standard applies to thermal transfer film for infusion soft bags made of plastic film as substrate and coated with transferable ink (hereinafter referred to as printing film).
2 Normative 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, parties to an agreement based on this standard are encouraged to study whether the latest versions of these documents can be used. For any undated referenced document, the latest version shall apply to this standard. GB/T191 Pictorial marking for packaging storage and transportation (idtISO780:1997) GB/T1040.3 Determination of tensile properties of plastics Part 3: Test conditions for films and sheets (idtISO527-3:1995) GB/T2918 Standard environment for conditioning and testing of plastic specimens (idtIS0291:1977) GB/T3979 Measurement method for object color
GB/T10004—2008 Plastic composite film, bag dry composite, extrusion composite for packaging GB/T12027—2004 Test method for dimensional change rate of plastic film and sheeting after heating (idtIS011501:1995) 3 Terms and definitions
The following terms and definitions apply to this standard. 3.1
Hot stamping foil for infusion bag is a kind of thermal transfer material used for printing the logo of infusion bag, which is made of plastic film as the base material and coated with transferable ink. 3.2
Mottle
Transparent spots appearing on the printed film due to production defects or other reasons. 3.3
Light line
Transparent straight-line pattern appearing on the printed film due to production defects or other reasons. 3.4
Lines
Dark straight-line pattern appearing on the printed film due to production defects or other reasons. 1
BB/T0051—2009
Foil tightness
Reflects the winding tension of the printed film roll, which is expressed by the surface hardness of the outer cylinder of the printed film roll. 3.6
Secondary transfer
The phenomenon that the print is abnormally adhered to the outer packaging film of the substrate and the surface of similar products. 3.7
Adhesion resistance
The property that the printing film and the substrate are easy to separate during the thermal transfer process. 4 Requirements
4.1 Specifications and dimensional deviation requirements
4.1.1 The commonly used specifications and dimensions of the printing film are shown in Table 1, and other specifications can be determined by negotiation between the supply and demand parties. Table 1
Common specifications and dimensions
The requirements for dimensional deviation of the printing film are shown in Table 2.
Width deviation
4.2 Appearance quality requirements
Width, mm
Table 2 Dimension deviation
4.2.1 The surface is not allowed to have stains, impurities, unevenness, and ribs, and interlayer adhesion is not allowed. Length, m
Length deviation
4.2.2 The end face is flat, no scratches or radial wrinkles are allowed, and the end face and the tube core are misaligned ≤2mm. 4.2.3 White stripes with a width of >0.5mm, white spots with a diameter of >1mm, and stripes with a width of >2mm are not allowed; the cumulative length of stripes with a width of ≤2mm is allowed to be no more than 5m/50m, the cumulative length of white stripes with a width of ≤0.5mm is allowed to be no more than 2m/50m, the diameter of white spots with a diameter of ≤1mm is allowed to be no more than 2/m2, and the number of joints is ≤2.
4.2.4 Color difference (CIEL*a*b*) requirements for the same batch and the same color: △E≤4. 4.2.5 The tightness of the film roll (Shore A) is required to be between 85 degrees and 98 degrees. 2
4.3 Product performance requirements
Product performance requirements are shown in Table 3.
Heat shrinkage (longitudinal)
Tensile strength
Anti-adhesion
Print clarity
Print friction resistance
Clarity after cooking
Print friction resistance after cooking
Secondary transfer
Ethanol resistance
4.4 Hygiene index requirements
4.4.1 The total amount of solvent residue is ≤10mg/m2. Table 3 Product performance requirements
Self-detachment
BB/T0051—2009
≥190
Clear line boundaries, no missing strokes or broken strokes, no burrs, ink clumps, or hollows
≥200
Clear line boundaries, no missing strokes or broken strokes, no burrs, ink clumps, or hollows
Clear line boundaries, no missing strokes or broken strokes, no burrs, ink clumps, or hollowsThe requirements for heavy metal content shall comply with relevant standards and laws and regulations. 4.4.2
5 Inspection method
5.1 Sampling method
After removing the packaging of the printed film roll, remove the sealing label and store it carefully to prevent contamination. 5.2 Sample Conditioning and Test Environment
The sample condition shall be conditioned in an environment of 23℃±5℃ and 50%±10% relative humidity as specified in CB/T2918 for not less than 8 hours, and the test shall be carried out under such environmental conditions. 5.3 Specification and Dimension Inspection
5.3.1 Width Inspection.
Unroll the printed film roll with the coating facing upward and lay it flat on a flat glass. In a tension-free state, measure at any 5 different positions with a measuring instrument with an accuracy of 1mm and take the arithmetic mean as the width of the printed film. 5.3.2 Length Inspection.
Inspect with a measuring instrument with an accuracy of not less than 5mm. 5.4 Appearance Quality Inspection
Under natural light, test according to 4.2.1~4.2.3. Visual inspection. 5.5 Inspection of color difference of the same color in the same batch
The instrument adopts an integrating sphere colorimeter, which shall comply with the provisions of GB/T3979. The standard illuminant is D65, and the color measurement field is 3
BB/T0051—2009
10°. The measurement area is generally a circular hole with a diameter of Φ25mm. If the measured part is small, a small area observation hole is allowed, and its area shall not be less than 25mm2.
Measure the L*α*b* value of the CIEL*α*b* uniform color space with the standard sample as the reference, and then measure the color difference AE of other samples and the same color standard sample.
5.6 Inspection of film roll tightness
Put the printed film roll flat, and use the Shore hardness tester to measure any position of the outer cylindrical surface of the printed film roll, and take the arithmetic average of the measurement results at 5 locations as the film roll tightness of the printed film roll. 5.7 Test of heat shrinkage (longitudinal)
Perform according to the test method of GB/T12027-2004. Test temperature is 150℃±3℃, heating time is 10min. 5.8 Test of tensile strength
Perform according to the provisions of GB/T1040.3. The specimen is in the shape of a strip with a length of 150mm and a width of 15mm±0.1mm, the distance between the clamps is 100mm, the tensile speed is 100mm/min±10mm/min, and 5 longitudinal specimens are measured respectively. 5.9 Test for anti-adhesion
According to the different materials of the infusion soft bag, install the medical PVC printing film, PVC film or medical non-PVC co-extruded printing film, non-PVC co-extruded film on the hot stamping machine, set the temperature to 120℃200℃; hot stamping pressure: 0.2MPa~0.6MPa; contact time: 0.1s~0.8s. Print automatically for 2m continuously, and visually check whether the printing film and the printing material can separate by themselves during the printing process. 5.10 Inspection of print clarity
According to the different materials of the infusion soft bag, install the medical PVC printing film, PVC film or medical non-PVC co-extruded printing film, non-PVC co-extruded film on the hot stamping machine, set the temperature to 120℃~200℃; hot stamping pressure: 0.2MPa~0.6MPa; contact time: 0.1s~0.8s, continuously and automatically print for 2m, and check the print on the substrate: graphic lines, missing strokes, broken strokes, burrs, ink clumps, hollows, and tailing phenomena.
5.11 Inspection of print friction resistance
Cut the copy paper into 50mm×220mm white paper strips and fix them on the sliding friction block of the testing machine with a load of 20N±0.2N; after turning on the machine, rub the print on the substrate back and forth at a uniform speed of 40 times/min, and record the number of frictions when the print begins to become blurred as the test result.
5.12 Test of resistance to boiling
Put the printed sample with intact imprint and tightly sealed with a packaging bag (PE or PP material) into the autoclave, add appropriate amount of water, and cook at 120℃~123℃ for 40min. After the cooking is completed, release the pressure, take the sample out of the autoclave, cool it to room temperature, and test the following indicators:
a) Determine the clarity of the imprint according to 5.10.
b) Determine the abrasion resistance of the imprint according to 5.11.
c) The phenomenon of secondary transfer of the imprint inside the outer packaging bag. 5.13 Test of resistance to ethanol
Take the sterilized sample in 5.12 and dry it, cut two 50mm×50mm samples (with imprints on them), soak them in 75% ethanol for 30min, take them out and dry them, and visually inspect the clarity of the imprint according to 5.10. 4
5.14 Inspection of the total amount of solvent residue
Carry out the test method specified in 6.6.17 of GB/T10004--2008. 6 Inspection rules
6.1 Batch
BB/T0051--2009
Products of the same specifications with the same raw materials, formula, process conditions, continuous production and simultaneous acceptance are considered a batch of 500 rolls. If the number is less than 500 rolls, the demand of one order is considered a batch. 6.2 Sampling
Randomly select 2 rolls from the same batch, of which 1 roll is reserved for sampling and 1 roll is inspected. 6.3 Inspection classification
Inspection is divided into factory inspection and type inspection.
6.3.1 Factory inspection. bZxz.net
Inspect the items in 4.1 and 4.2, and inspect the items in 4.3 except for the tensile strength and thermal shrinkage rate. 6.3.2 Type inspection.
Type inspection items are all inspection items required in Chapter 4. Type inspection shall be carried out in any of the following situations: a) Trial production of new products or old products for transfer to other factories; b) After formal production, when the ink formula, raw materials, production process, and production equipment have major changes that may affect product performance; c) During formal production, inspection shall be carried out once a year after regular or accumulated production; d) When the product is stopped for more than two months and production is resumed; when the factory inspection result is significantly different from the previous routine inspection result; e)
When the national quality supervision agency proposes a type inspection requirement; g)
When the user proposes an inspection requirement in the order contract. 6.3.3 Judgment rules
Specifications, dimensions, appearance quality, and product performance shall be inspected in accordance with the requirements of 4.1~4.4. If one of 4.1 and 4.2 is unqualified, double sampling shall be carried out for re-inspection. If all are qualified, it shall be judged as qualified, and if one is unqualified, it shall be judged as unqualified; if one of 4.3 and 4.4 is unqualified, the batch shall be judged as unqualified.
7 Marking, packaging, transportation and storage
7.1 Marking
According to the provisions of GB191, each product shall be affixed with a label printed with the product name, number, specification, certificate of conformity, production date and other relevant information.
7.2 Packaging
The product shall be placed in a transparent plastic bag and sealed. 7.3 Transportation
The product shall be transported by a canopy. It is not allowed to be thrown, dropped, lost or thrown during transportation. Avoid squeezing, impact, sun exposure and rain.
7.4 Storage
7.4.1 The product shall be stored in a dry, ventilated room without corrosive substances such as acid and alkali. The temperature should be kept at 5℃~35℃ and the relative humidity should not be higher than 85%.
7.4.2 When stacking products, they should be placed on a flat ground or board in the direction indicated by the arrow on the carton, 1m away from the heat source, and the products should remain in their original packaging state. The stacking height should not exceed 1.2m. The storage period shall not exceed 12 months from the date of production. 7.4.3
S/N:1580177·313
911580171731309
Packaging Industry Standard of the People's Republic of China
Thermal Transfer Film for Infusion Soft Bags
BB/T0051—2009
Published by China Planning Press
(Address: 4th Floor, Building C, Guohong Building, No. 11 Mudi Beilijia, Xicheng District, Beijing) (Postal Code ：100038Tel: 6390643363906381)
Published by Beijing Xinhua Bookstore
Printed by Sanhe Fuhua Printing and Packaging Co., Ltd.880×1230 mm1/160.75 Sheet13,000 wordsFirst edition in January 2010First printing in January 2010Print run 1-600 copies
Unified book number: 1580177·313
Copyright exclusiveInfringements will be investigated9. Test for anti-adhesion
According to the different materials of the infusion soft bag, install the medical PVC printing film, PVC film or medical non-PVC co-extruded printing film, non-PVC co-extruded film on the hot stamping machine, set the temperature to 120℃200℃; hot stamping pressure: 0.2MPa~0.6MPa; contact time: 0.1s~0.8s. Continuously print automatically for 2m, and visually check whether the printing film and the printing material can separate by themselves during the printing process. 5.10 Inspection of print clarity
According to the different materials of the infusion soft bag, install the medical PVC printing film, PVC film or medical non-PVC co-extruded printing film, non-PVC co-extruded film on the hot stamping machine, set the temperature to 120℃~200℃; hot stamping pressure: 0.2MPa~0.6MPa; contact time: 0.1s~0.8s, continuously and automatically print for 2m, and check the print on the substrate: graphic lines, missing strokes, broken strokes, burrs, ink clumps, hollows, and tailing phenomena.
5.11 Inspection of print friction resistance
Cut the copy paper into 50mm×220mm white paper strips and fix them on the sliding friction block of the testing machine with a load of 20N±0.2N; after turning on the machine, rub the print on the substrate back and forth at a uniform speed of 40 times/min, and record the number of frictions when the print begins to become blurred as the test result.
5.12 Test of resistance to boiling
Put the printed sample with intact imprint and tightly sealed with a packaging bag (PE or PP material) into the autoclave, add appropriate amount of water, and cook at 120℃~123℃ for 40min. After the cooking is completed, release the pressure, take the sample out of the autoclave, cool it to room temperature, and test the following indicators:
a) Determine the clarity of the imprint according to 5.10.
b) Determine the abrasion resistance of the imprint according to 5.11.
c) The phenomenon of secondary transfer of the imprint inside the outer packaging bag. 5.13 Test of resistance to ethanol
Take the sterilized sample in 5.12 and dry it, cut two 50mm×50mm samples (with imprints on them), soak them in 75% ethanol for 30min, take them out and dry them, and visually inspect the clarity of the imprint according to 5.10. 4
5.14 Inspection of the total amount of solvent residue
Carry out the test method specified in 6.6.17 of GB/T10004--2008. 6 Inspection rules
6.1 Batch
BB/T0051--2009
Products of the same specifications with the same raw materials, formula, process conditions, continuous production and simultaneous acceptance are considered a batch of 500 rolls. If the number is less than 500 rolls, the demand of one order is considered a batch. 6.2 Sampling
Randomly select 2 rolls from the same batch, of which 1 roll is reserved for sampling and 1 roll is inspected. 6.3 Inspection classification
Inspection is divided into factory inspection and type inspection.
6.3.1 Factory inspection.
Inspect the items in 4.1 and 4.2, and inspect the items in 4.3 except for the tensile strength and thermal shrinkage rate. 6.3.2 Type inspection.
Type inspection items are all inspection items required in Chapter 4. Type inspection shall be carried out in any of the following situations: a) Trial production of new products or old products for transfer to other factories; b) After formal production, when the ink formula, raw materials, production process, and production equipment have major changes that may affect product performance; c) During formal production, inspection shall be carried out once a year after regular or accumulated production; d) When the product is stopped for more than two months and production is resumed; when the factory inspection result is significantly different from the previous routine inspection result; e)
When the national quality supervision agency proposes a type inspection requirement; g)
When the user proposes an inspection requirement in the order contract. 6.3.3 Judgment rules
Specifications, dimensions, appearance quality, and product performance shall be inspected in accordance with the requirements of 4.1~4.4. If one of 4.1 and 4.2 is unqualified, double sampling shall be carried out for re-inspection. If all are qualified, it shall be judged as qualified, and if one is unqualified, it shall be judged as unqualified; if one of 4.3 and 4.4 is unqualified, the batch shall be judged as unqualified.
7 Marking, packaging, transportation and storage
7.1 Marking
According to the provisions of GB191, each product shall be affixed with a label printed with the product name, number, specification, certificate of conformity, production date and other relevant information.
7.2 Packaging
The product shall be placed in a transparent plastic bag and sealed. 7.3 Transportation
The product shall be transported by a canopy. It is not allowed to be thrown, dropped, lost or thrown during transportation. Avoid squeezing, impact, sun exposure and rain.
7.4 Storage
7.4.1 The product shall be stored in a dry, ventilated room without corrosive substances such as acid and alkali. The temperature should be kept at 5℃~35℃ and the relative humidity should not be higher than 85%.
7.4.2 When stacking products, they should be placed on a flat ground or board in the direction indicated by the arrow on the carton, 1m away from the heat source, and the products should remain in their original packaging state. The stacking height should not exceed 1.2m. The storage period shall not exceed 12 months from the date of production. 7.4.3
S/N:1580177·313
911580171731309
Packaging Industry Standard of the People's Republic of China
Thermal Transfer Film for Infusion Soft Bags
BB/T0051—2009
Published by China Planning Press
(Address: 4th Floor, Building C, Guohong Building, No. 11 Mudi Beilijia, Xicheng District, Beijing) (Postal Code ：100038Tel: 6390643363906381)
Published by Beijing Xinhua Bookstore
Printed by Sanhe Fuhua Printing and Packaging Co., Ltd.880×1230 mm1/160.75 Sheet13,000 wordsFirst edition in January 2010First printing in January 2010Print run 1-600 copies
Unified book number: 1580177·313
Copyright exclusiveInfringements will be investigated9. Test for anti-adhesion
According to the different materials of the infusion soft bag, install the medical PVC printing film, PVC film or medical non-PVC co-extruded printing film, non-PVC co-extruded film on the hot stamping machine, set the temperature to 120℃200℃; hot stamping pressure: 0.2MPa~0.6MPa; contact time: 0.1s~0.8s. Continuously print automatically for 2m, and visually check whether the printing film and the printing material can separate by themselves during the printing process. 5.10 Inspection of print clarity
According to the different materials of the infusion soft bag, install the medical PVC printing film, PVC film or medical non-PVC co-extruded printing film, non-PVC co-extruded film on the hot stamping machine, set the temperature to 120℃~200℃; hot stamping pressure: 0.2MPa~0.6MPa; contact time: 0.1s~0.8s, continuously and automatically print for 2m, and check the print on the substrate: graphic lines, missing strokes, broken strokes, burrs, ink clumps, hollows, and tailing phenomena.
5.11 Inspection of print friction resistance
Cut the copy paper into 50mm×220mm white paper strips and fix them on the sliding friction block of the testing machine with a load of 20N±0.2N; after turning on the machine, rub the print on the substrate back and forth at a uniform speed of 40 times/min, and record the number of frictions when the print begins to become blurred as the test result.
5.12 Test of resistance to boiling
Put the printed sample with intact imprint and tightly sealed with a packaging bag (PE or PP material) into the autoclave, add appropriate amount of water, and cook at 120℃~123℃ for 40min. After the cooking is completed, release the pressure, take the sample out of the autoclave, cool it to room temperature, and test the following indicators:
a) Determine the clarity of the imprint according to 5.10.
b) Determine the abrasion resistance of the imprint according to 5.11.
c) The phenomenon of secondary transfer of the imprint inside the outer packaging bag. 5.13 Test of resistance to ethanol
Take the sterilized sample in 5.12 and dry it, cut two 50mm×50mm samples (with imprints on them), soak them in 75% ethanol for 30min, take them out and dry them, and visually inspect the clarity of the imprint according to 5.10. 4
5.14 Inspection of the total amount of solvent residue
Carry out the test method specified in 6.6.17 of GB/T10004--2008. 6 Inspection rules
6.1 Batch
BB/T0051--2009
Products of the same specifications with the same raw materials, formula, process conditions, continuous production and simultaneous acceptance are considered a batch of 500 rolls. If the number is less than 500 rolls, the demand of one order is considered a batch. 6.2 Sampling
Randomly select 2 rolls from the same batch, of which 1 roll is reserved for sampling and 1 roll is inspected. 6.3 Inspection classification
Inspection is divided into factory inspection and type inspection.
6.3.1 Factory inspection.
Inspect the items in 4.1 and 4.2, and inspect the items in 4.3 except for the tensile strength and thermal shrinkage rate. 6.3.2 Type inspection.
Type inspection items are all inspection items required in Chapter 4. Type inspection shall be carried out in any of the following situations: a) Trial production of new products or old products for transfer to other factories; b) After formal production, when the ink formula, raw materials, production process, and production equipment have major changes that may affect product performance; c) During formal production, inspection shall be carried out once a year after regular or accumulated production; d) When the product is stopped for more than two months and production is resumed; when the factory inspection result is significantly different from the previous routine inspection result; e)
When the national quality supervision agency proposes a type inspection requirement; g)
When the user proposes an inspection requirement in the order contract. 6.3.3 Judgment rules
Specifications, dimensions, appearance quality, and product performance shall be inspected in accordance with the requirements of 4.1~4.4. If one of 4.1 and 4.2 is unqualified, double sampling shall be carried out for re-inspection. If all are qualified, it shall be judged as qualified, and if one is unqualified, it shall be judged as unqualified; if one of 4.3 and 4.4 is unqualified, the batch shall be judged as unqualified.
7 Marking, packaging, transportation and storage
7.1 Marking
According to the provisions of GB191, each product shall be affixed with a label printed with the product name, number, specification, certificate of conformity, production date and other relevant information.
7.2 Packaging
The product shall be placed in a transparent plastic bag and sealed. 7.3 Transportation
The product shall be transported by a canopy. It is not allowed to be thrown, dropped, lost or thrown during transportation. Avoid squeezing, impact, sun exposure and rain.
7.4 Storage
7.4.1 The product shall be stored in a dry, ventilated room without corrosive substances such as acid and alkali. The temperature should be kept at 5℃~35℃ and the relative humidity should not be higher than 85%.
7.4.2 When stacking products, they should be placed on a flat ground or board in the direction indicated by the arrow on the carton, 1m away from the heat source, and the products should remain in their original packaging state. The stacking height should not exceed 1.2m. The storage period shall not exceed 12 months from the date of production. 7.4.3
S/N:1580177·313
911580171731309
Packaging Industry Standard of the People's Republic of China
Thermal Transfer Film for Infusion Soft Bags
BB/T0051—2009
Published by China Planning Press
(Address: 4th Floor, Building C, Guohong Building, No. 11 Mudi Beilijia, Xicheng District, Beijing) (Postal Code ：100038Tel: 6390643363906381)
Published by Beijing Xinhua Bookstore
Printed by Sanhe Fuhua Printing and Packaging Co., Ltd.880×1230 mm1/160.75 Sheet13,000 wordsFirst edition in January 2010First printing in January 2010Print run 1-600 copies
Unified book number: 1580177·313
Copyright exclusiveInfringements will be investigated3 except for the tensile strength and heat shrinkage items. 6.3.2 Type inspection.
Type inspection items are all the inspection items required in Chapter 4. Type inspection shall be carried out in any of the following situations: a) Trial production of new products or old products transferred to the factory for production; b) After formal production, the ink formula, raw materials, production process, and production equipment have major changes that may affect product performance; c) During formal production, inspections are carried out once a year on a regular basis or after accumulating a certain amount of output; d) When the product is discontinued for more than two months and production is resumed; when the factory inspection results are significantly different from the last routine inspection results; e)
When the national quality supervision agency proposes a type inspection requirement; g)
When the user proposes an inspection requirement in the order contract. 6.3.3 Judgment rules
Specifications, dimensions, appearance quality, and product performance shall be inspected in accordance with the requirements of 4.1~4.4. If one of 4.1 and 4.2 is unqualified, double sampling shall be conducted for re-inspection. If all are qualified, it shall be qualified, and if one is unqualified, it shall be unqualified; if one of 4.3 and 4.4 is unqualified, the batch shall be judged unqualified.
7 Marking, packaging, transportation and storage
7.1 Marking
According to the provisions of GB191, each product shall be affixed with a label printed with relevant information such as product name, number, specification, certificate of conformity, production date, etc.
7.2 Packaging
Products shall be placed in transparent plastic bags and sealed. 7.3 Transportation
The products should be transported by covered transport vehicles. The products are not allowed to be thrown, dropped, dropped or thrown during transportation. They should be kept away from extrusion, impact, sun exposure and rain.
7.4 Storage
7.4.1 The products should be stored in a dry, ventilated room without acid, alkali and other corrosive substances. The temperature should be kept at 5℃~35℃ and the relative humidity should not be higher than 85%.
7.4.2 When stacking the products, they should be placed on a flat ground or on a board in the direction indicated by the arrow on the carton, and 1m away from the heat source. The products should be kept in the original packaging state and the stacking height should not exceed 1.2m. The storage period shall not exceed 12 months from the date of production. 7.4.3
S/N:1580177·313
911580171731309
Packaging Industry Standard of the People's Republic of China
Thermal Transfer Film for Infusion Soft Bags
BB/T0051—2009
Published by China Planning Press
(Address: 4th Floor, Building C, Guohong Building, No. 11, Mudi Beilijia, Xicheng District, Beijing) (Postal Code ：100038Tel: 6390643363906381)
Published by Beijing Xinhua Bookstore
Printed by Sanhe Fuhua Printing and Packaging Co., Ltd.880×1230 mm1/160.75 Sheet13,000 wordsFirst edition in January 2010First printing in January 2010Print run 1-600 copies
Unified book number: 1580177·313
Copyright exclusiveInfringements will be investigated3 except for the tensile strength and heat shrinkage items. 6.3.2 Type inspection.
Type inspection items are all the inspection items required in Chapter 4. Type inspection shall be carried out in any of the following situations: a) Trial production of new products or old products transferred to the factory for production; b) After formal production, the ink formula, raw materials, production process, and production equipment have major changes that may affect product performance; c) During formal production, inspections are carried out once a year on a regular basis or after accumulating a certain amount of output; d) When the product is discontinued for more than two months and production is resumed; when the factory inspection results are significantly different from the last routine inspection results; e)
When the national quality supervision agency proposes a type inspection requirement; g)
When the user proposes an inspection requirement in the order contract. 6.3.3 Judgment rules
Specifications, dimensions, appearance quality, and product performance shall be inspected in accordance with the requirements of 4.1~4.4. If one of 4.1 and 4.2 is unqualified, double sampling shall be conducted for re-inspection. If all are qualified, it shall be qualified, and if one is unqualified, it shall be unqualified; if one of 4.3 and 4.4 is unqualified, the batch shall be judged unqualified.
7 Marking, packaging, transportation and storage
7.1 Marking
According to the provisions of GB191, each product shall be affixed with a label printed with relevant information such as product name, number, specification, certificate of conformity, production date, etc.
7.2 Packaging
Products shall be placed in transparent plastic bags and sealed. 7.3 Transportation
The products should be transported by covered transport vehicles. The products are not allowed to be thrown, dropped, dropped or thrown during transportation. They should be kept away from extrusion, impact, sun exposure and rain.
7.4 Storage
7.4.1 The products should be stored in a dry, ventilated room without acid, alkali and other corrosive substances. The temperature should be kept at 5℃~35℃ and the relative humidity should not be higher than 85%.
7.4.2 When stacking the products, they should be placed on a flat ground or on a board in the direction indicated by the arrow on the carton, and 1m away from the heat source. The products should be kept in the original packaging state and the stacking height should not exceed 1.2m. The storage period shall not exceed 12 months from the date of production. 7.4.3
S/N:1580177·313
911580171731309
Packaging Industry Standard of the People's Republic of China
Thermal Transfer Film for Infusion Soft Bags
BB/T0051—2009
Published by China Planning Press
(Address: 4th Floor, Building C, Guohong Building, No. 11, Mudi Beilijia, Xicheng District, Beijing) (Postal Code ：100038Tel: 6390643363906381)
Published by Beijing Xinhua Bookstore
Printed by Sanhe Fuhua Printing and Packaging Co., Ltd.880×1230 mm1/160.75 Sheet13,000 wordsFirst edition in January 2010First printing in January 2010Print run 1-600 copies
Unified book number: 1580177·313
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