JB 20024-2004 Automatic traditional Chinese medicine pill making machine
Some standard content:
JB | |Rolling mode soft capsule machine
Capsule tablet printing machine
Released on 2004-02-05
Implemented on 2004-06-01
Released by the National Development and Reform Commission|| tt | Pill machine
Chinese traditional medicine automatic pill making machine2004-02-05 release
2004-06-01 implementation
National Development and Reform Commission release
Foreword||tt ||1 Scope
2 Normative reference documents
3 Classification and labeling
4 Requirements
5 Test methods
6 Inspection rules||tt| |7
Logo, instruction manual, packaging, transportation and storage
times
JB20024—2004
JB20024—2004
Foreword| ||This standard is based on the requirements of the "Good Manufacturing Practice for Pharmaceutical Products" and CB/T1.1-2000, GB/T1.2--2002 Standardization Work Guidelines, and is based on YY0023-1990 "Automatic Pill Making Machine for Traditional Chinese Medicine" Revision. This standard replaces YY0023-1990 from the date of implementation. Compared with YY0023~-1990, the main technical content changes of this standard are as follows: the main chapters and clauses in YY00231990 have been deleted; a)
—Basic requirements (4.1);
—Casting dimensional accuracy ( 4.2);
—Metal plating (4.4.1);
Paint quality (4.4.2).
Revised the main chapters and articles in YY0023-1990: b)
Reference standards (Chapter 2);
Requirements (Chapter 4);
Test Methods (Chapter 5);
Testing rules (Chapter 6).
c) Main chapters and clauses added to this standard:
4.2.3, 4.3.1, 4.3.2.4.4.1, 4.4.2.4.4.3.4.5, 4.6.3, 4.7, 4.8 .3. 4.10.4 This standard is proposed by China Pharmaceutical Equipment Industry Association. This standard is under the jurisdiction of the Pharmaceutical Equipment Industry Standardization Technical Committee. This standard was drafted by: Heilongjiang Deere Pharmaceutical Machinery Co., Ltd. The main drafters of this standard: Lu Zhiqing, Li Hongcai, Gao Chuan, Xu Xingguo, Guo Wansheng. 4
1 Scope
Automatic pill-making machine for traditional Chinese medicine
JB20024—2004
This standard specifies the classification and labeling, requirements, test methods, Inspection rules and markings, instructions for use, packaging, transportation and storage.
This standard applies to automatic traditional Chinese medicine pill making machines (referred to as pill making machines). 2 Normative reference documents
The provisions in the following documents become provisions of this standard through reference in this standard. For referenced documents with a reference period, all subsequent amendments (excluding corrigenda) or revisions do not apply to this standard. However, parties that reach an agreement based on this standard are encouraged to study whether the latest versions of these documents can be used. . For any referenced document with no expiration date, the latest version shall apply to this standard. GB/T191 Pictorial signs for packaging, storage and transportation
GB/T9969.1 General instructions for industrial products
GB/T13306 Signs
GB/T13384 General technical conditions for mechanical and electrical product packaging CB/T16769 Metal cutting machine tool noise and compression measurement method GB5226.1-2002 Machinery Safety Mechanical and Electrical Equipment Part 1: General Technical Conditions GB/T10111 Random sampling method using random numbers GB/T6388 Transport stall packaging receipt and delivery marks | |tt||YY/T0216 Pharmaceutical Machinery Product Model Preparation Method Pharmacopoeia of the People's Republic of China (2000 Edition) National Pharmacopoeia Commission Good Manufacturing Practice (1998 Revised Edition) State Food and Drug Administration 3 Classification and Labeling
3.1 Type , Main structure
3.1.1 Type: vertical, horizontal.
3.1.2 Main structure: The pill making machine consists of a feeding mechanism, a strip dispensing mechanism, a cutting and rolling forming mechanism, an automatic control mechanism and a roller brush anti-sticking mechanism. 3.2 Model
The model compilation method is in accordance with the provisions of YY/T0216. JB20024—2004
Wz
Marking example:
W
120
Improved design sequence number: A, B, C..||tt| |Specification code, maximum production capacity, kg/h (6mm in pills, Shuicui pills, 0=1.5g/cm) Type code: vertical one - L, horizontal one W Chinese medicine
Function code, pills Machinery
A
First improved design
Maximum production capacity, kg/h (pellet 6mm, watertight pill, D=1.5g/cm\) Vertical||tt| |TCM
Pills
w..zZ.W-120
A
First improved design
Maximum production capacity, kg/h ( Pills Φ6rmm, water honey pills, 0=1.5g/cm\) horizontal
traditional Chinese medicine
pills
4 requirements
4.1 All parts in contact with drugs should be It is made of materials that are particularly toxic, corrosion-resistant, and do not chemically change with or adsorb drugs. 4.2 Appearance requirements for the entire machine
4.2.1 The surface of the sheet metal parts must not have scratches or uneven convex and concave defects. 4.2.2 The outer surface should be smooth and smooth, without burrs or sharp edges. 4.2.3 The feeding mechanism, strip dispensing mechanism, and cutting and rolling pill making mechanism should be installed with sealed transparent protective covers. 4.3 Feeding mechanism requirements
4.3.1 Feed the material evenly.
4.3.2 The feeding mechanism can be quickly disassembled and easy to clean. 4.4 Requirements for the sliver dispensing mechanism
4.4.1 Multiple sliver dispensing speeds must be synchronized and consistent.
4.4.2 The gap between the inner diameter of the delivery can and the outer diameter of the explosive spin propeller is 0.5mm~0.8mm; the gap between the end face of the delivery can and the end face of the explosive spin propeller is 1.0mm~1.5mm.
4.4.3 The strip delivery mechanism can be quickly disassembled and easy to clean. 6
4.5 The automatic control mechanism is sensitive and reliable.
4.6 Requirements for the cutting and rolling pill-making mechanism
4.6.1 The pill-making mechanism is stable and reliable, and the gap between the pill-making knives is 0.02mm~0.10mm. JB 20024-2004
4.6.2 The radial runout of the cutter shaft is less than 0.05mm, the parallelism of the two cutter shafts is less than 0.05mm, and the center distance of the pill-making knife shaft is 1268 mm4.6.3 The speed of the pill-making knife can be stepless The speed is adjustable and the pill making knife can be quickly disassembled and easy to clean. 4.7 Requirements for roller brush anti-adhesion mechanism
4.7.1 The steering direction of the falling brush is consistent with the steering direction of the pill-making knife. 4.7.2 The roller brush rotates flexibly, and the interference between the outer diameter of the roller brush and the pill-making knife is 0.3mm~0.5mm. 4.8 Assembly quality requirements
4.8.1 Each transmission part should rotate smoothly without looseness, and the noise under load should not exceed 75dB(A). The joint between each rotating shaft and the sealing surface should be sealed reliably and there should be no oil leakage. 4.8.2
4.8.3 The lubricant channel is reliably sealed and has no leakage. 4.8.4 The temperature rise of rolling bearings shall not exceed 35°C. 4.8.5 The overflow of the transmission box and reduction box shall not exceed 35℃. 4.8.6 The idle running current shall not exceed 63% of the rated current. 4.9 Performance requirements
4.9.1 The pill making machine should use lubricants that meet the process and equipment requirements. 4.9.2 The weight difference of pills complies with the provisions of the General Preparations (Pills) in the Pharmacopoeia of the People's Republic of China (2000 Edition). 4.9.3 The pills have an even shape and consistent color, and the pass rate is not less than 95%. 4.10 Electrical system safety requirements
4.10.1 The continuity of the protective grounding of the electrical system shall comply with the provisions of 19.2 in CB5226.1-2002. 4.10.2 The insulation resistance of the electrical system should comply with the provisions of 19.3 in GB5226.1-2002. 4.10.3 The withstand voltage of the electrical system should comply with CB5226.The provisions of 19.4 of 1-2002. 4.10.4 The protective grounding circuit of the electrical system should comply with the provisions of 8.2 in CB5226.1-2002. 4.10.5 The buttons of the electrical system should comply with the provisions of 10.2 in GB5226.1-2002. 4.10.6 The indicators and displays of the electrical system should comply with the provisions of 10.3 in GB5226.1-2002. 4.10.7 The wiring of the electrical system should comply with the provisions of Chapter 14 of CB5226.1-2002. The markings, warning signs and project codes of the electrical system shall comply with the provisions of Chapter 17 of GB5226.1--2002. 4.10.8
5 Test methods
5.1 Materials of parts in contact with drugs should have material certification. When there is no material certificate, the manufacturer should inspect and confirm the material. 5.2 Appearance. The outer surface of the whole machine and the surface of the sheet metal parts should be visually inspected. 5.3 Inspection of feeding mechanism. Visually inspect feed uniformity. 5.4 Inspection of the strip discharging mechanism
5.4.1 Use visual inspection to inspect the synchronicity of multiple strips coming out. 5.4.2 Use a vernier caliper to measure the gap between the inner diameter of the can and the outer diameter of the screw propeller, and the gap between the end face of the strip outlet and the end face of the screw propeller.
7
.JB20024—2004
5.5 Automatic control mechanism inspection. Use visual inspection to observe the ammeter and voltmeter to check whether the control is sensitive and reliable. 5.6 Inspection of pill making institutions. Use a feeler gauge to measure the gap of the pill making knife. Use a micrometer to measure the center distance of the pill-making knife shaft in a static state. Start the pill-making knife shaft and stop after rotating 180 degrees. Use a dry ruler to measure the center distance of the pill-making knife shaft. 5.7 Assembly quality
5.7.1 Dry running test.
5.7.1.1 The dry running test time shall not be less than 60 minutes. During the dry running test, check the rotation of each transmission part and the stability and reliability of the pill making mechanism.
5.7.1.2 Use a clamp-type ammeter to detect the no-load current. 5.7.1.3 During dry operation, use a dial indicator to measure the radial runout of the cutter shaft and the parallelism of the cutter shaft. 5.7.2 Noise test. Use a sound level meter to detect the load noise of the pill making machine according to the regulations in GB/T16769. 5.7.3 Load test.
5.7.3.1 The load test shall be carried out after the dry running test, and the test time shall not be less than 120 minutes. 5.7.3.2 The temperature rise of the transmission box and reduction box is measured with a thermometer. 5.7.3.3 The temperature rise of the bearing is measured on the bearing shell with a thermometer. 5.8 Inspection of performance
5.8.1 The appearance quality of the pills and the lubricant used should be visually inspected. 5.8.2 The weight difference of pills complies with the provisions of the General Preparations (Pills) in the Pharmacopoeia of the People's Republic of China (2000 Edition), and the weight difference limit is checked according to the second method. If the pills need to be sugar-coated, the weight difference of the pill cores should be checked before coating, and the weight difference should not be checked after sugar-coating.
5.8.3 The passing rate of pills is tested by sampling method: 10 groups of 100 pills in each group are randomly selected from the produced pills for visual inspection. 5.9 Electrical system safety test methods
5.9.1 The continuity, insulation resistance and withstand voltage tests of the protective grounding circuit of the electrical system shall be tested in accordance with the provisions of 19.219.3 and 19.4 in GB5226.1-2002 respectively.
5.9.2 The protective grounding circuit, buttons, indicators and displays, wiring, markings, warning signs and project codes of the electrical system shall be in accordance with GB5226.1-2002 8.2, 10.2, 10.3, Chapter 14 and Check the provisions of Chapter 17. 6 Inspection Rules
The inspection of pill making machines is divided into factory inspection and type inspection. 6.1 Factory inspection
6.1.1 Before leaving the factory, the pill making machine shall be inspected one by one according to the provisions of Table 1. Only if it is qualified will it be allowed to leave the factory, and a product certificate shall be attached. Table 1 Factory inspection items
Item categories
General items
Main items
Inspection items
4.2, 4.3, 4.4.1, 4.4. 3, 4.5, 4.6.3, 4.8.2, 4.8.4, 4.8.54.1,4.4.2, 4.6.1,4.6.2, 4.7,4.8.1,4.8.3,4.8.6,4.9, 4.106. 1.2 During the inspection process, if the pill making machine is found to be unqualified, it should be returned for repair. After repair, it should be re-inspected. If it is still unqualified, the product will be judged as unqualified.
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6.2 Type Inspection
6.2.1 Type inspection is required in any of the following situations: a) When the important structural design, process or material changes of the product may affect the product When the performance and safety of the product are: b) When the factory inspection results are significantly different from the last type test: c) When the national quality supervision agency proposes type inspection. 6.2.2 Type inspection items include all requirements of this standard. JB 20024—2004
6.2.3 Sampling. The prototype for type inspection shall be selected from 10% (depending on the situation) of the products that have passed the factory inspection according to the method specified in GB/T10111, and one unit shall be tested.
6.2.4 Determination rules. During the type inspection, if any of the electrical safety performance protective grounding circuit continuity, insulation resistance, and withstand voltage tests fails, the product will be judged to have failed the type inspection. If one of the other items is unqualified, the unqualified item should be retested twice. If it is still unqualified, the product will be judged to have failed the type inspection. 7 Logo, instructions for use, packaging, transportation and storage 7.1 Logo
7.1.1 The product should have a product label fixed at the position specified on the drawing, and the label should comply with the regulations of CB/T13306. The sign should include the following content:
a) Product name and model:
b) Main parameters;
Manufacturer name:
c)
d )
factory number;
e)
factory date:
f) product standard number.
7.1.2
The text and markings on the outer wall of the packaging box should be clear. 7.1.2.1 Storage and transportation signs shall comply with the provisions of GB/T191, including the words "upward" and "no turning over paint" or signs. 7.1.2.2 Transportation packaging and receipt signs shall comply with the provisions of CB/T6388, and include the following: a ) Product name, model;
Shipping date:
b)
Wooden box dimensions;
c
d)
Net weight and gross weight:
e) Shipping and receiving station names;
Sending and receiving units.
7.2 Instructions for use
Product instructions for use should comply with GB/T9969. The provisions of .1 should include the following content: a) product model and name, manufacturing unit name, address, postal code and contact number; implemented product standards;
b)
c) working conditions, Power supply, climate environment (such as temperature and humidity, atmospheric pressure, air cleanliness), etc.: d) The main structure, performance, specifications, uses, precautions, warnings and reminders, and safety measures of the product;1. The dry running test time shall be no less than 60 minutes. During the dry running test, check the rotation of each transmission part and the stability and reliability of the pill making mechanism.
5.7.1.2 Use a clamp-type ammeter to detect the no-load current. 5.7.1.3 During dry operation, use a dial indicator to measure the radial runout of the cutter shaft and the parallelism of the cutter shaft. 5.7.2 Noise test. Use a sound level meter to detect the load noise of the pill making machine according to the regulations in GB/T16769. 5.7.3 Load test.
5.7.3.1 The load test shall be carried out after the dry running test, and the test time shall not be less than 120 minutes. 5.7.3.2 The temperature rise of the transmission box and reduction box is measured with a thermometer. 5.7.3.3 The temperature rise of the bearing is measured on the bearing shell with a thermometer. 5.8 Inspection of performance
5.8.1 The appearance quality of the pills and the lubricant used should be visually inspected. 5.8.2 The weight difference of pills complies with the provisions of the General Preparations (Pills) in the Pharmacopoeia of the People's Republic of China (2000 Edition), and the weight difference limit is checked according to the second method. If the pills need to be sugar-coated, the weight difference of the pill cores should be checked before coating, and the weight difference should not be checked after sugar-coating.
5.8.3 The passing rate of pills is tested by sampling method: 10 groups of 100 pills in each group are randomly selected from the produced pills for visual inspection. 5.9 Electrical system safety test methods
5.9.1 The continuity, insulation resistance and withstand voltage tests of the protective grounding circuit of the electrical system shall be tested in accordance with the provisions of 19.219.3 and 19.4 in GB5226.1-2002 respectively.
5.9.2 The protective grounding circuit, buttons, indicators and displays, wiring, markings, warning signs and project codes of the electrical system shall be in accordance with GB5226.1-2002 8.2, 10.2, 10.3, Chapter 14 and Check the provisions of Chapter 17. 6 Inspection Rules
The inspection of pill making machines is divided into factory inspection and type inspection. 6.1 Factory inspection
6.1.1 Before leaving the factory, the pill making machine shall be inspected one by one according to the provisions of Table 1. Only if it is qualified will it be allowed to leave the factory, and a product certificate shall be attached. Table 1 Factory inspection items
Item categories
General items
Main items
Inspection items
4.2, 4.3, 4.4.1, 4.4. 3, 4.5, 4.6.3, 4.8.2, 4.8.4, 4.8.54.1,4.4.2, 4.6.1,4.6.2, 4.7,4.8.1,4.8.3,4.8.6,4.9, 4.106. 1.2 During the inspection process, if the pill making machine is found to be unqualified, it should be returned for repair. After repair, it should be re-inspected. If it is still unqualified, the product will be judged as unqualified.
8
6.2 Type Inspection
6.2.1 Type inspection is required in any of the following situations: a) When the important structural design, process or material changes of the product may affect the product When the performance and safety of the product are: b) When the factory inspection results are significantly different from the last type test: c) When the national quality supervision agency proposes type inspection. 6.2.2 Type inspection items include all requirements of this standard. JB 20024—2004
6.2.3 Sampling. The prototype for type inspection shall be selected from 10% (depending on the situation) of the products that have passed the factory inspection according to the method specified in GB/T10111, and one unit shall be tested.
6.2.4 Determination rules. During the type inspection, if any of the protective grounding circuit continuity, insulation resistance, and withstand voltage tests in the electrical safety performance fails, the product will be judged to have failed the type inspection. If one of the other items is unqualified, the unqualified item should be retested twice. If it is still unqualified, the product will be judged to have failed the type inspection. 7 Logo, instructions for use, packaging, transportation and storage 7.1 Logo
7.1.1 The product should have a product label fixed at the position specified on the drawing, and the label should comply with the regulations of CB/T13306. The sign should include the following content:
a) Product name and model:
b) Main parameters;
Manufacturer name:
c)
d )
factory number;
e)
factory date:
f) product standard number.
7.1.2
The text and markings on the outer wall of the packaging box should be clear. 7.1.2.1 Storage and transportation signs shall comply with the provisions of GB/T191, including the words "upward" and "no turning over paint" or signs. 7.1.2.2 The transportation packaging, receipt and delivery signs shall comply with the provisions of CB/T6388, and include the following: a ) Product name, model;
Shipping date:
b)
Overall dimensions of wooden box;
c
d)
Net weight and gross weight:
e) Shipping and receiving station names;
Sending and receiving units.
7.2 Instructions for use
Product instructions for use should comply with GB/T9969. The provisions of .1 should include the following: a) product model and name, manufacturing unit name, address, postal code and contact number; implemented product standards;
b)
c) working conditions, Power supply, climate environment (such as temperature and humidity, atmospheric pressure, air cleanliness), etc.: d) The main structure, performance, specifications, uses, precautions, warnings and reminder instructions, and safety measures of the product;1 The idle running test time shall not be less than 60 minutes. During the idle running test, check the rotation of each transmission part, the stability and reliability of the pill making mechanism.
5.7.1.2 Use a clamp-on ammeter to detect the no-load current. 5.7.1.3 During the idle running, use a micrometer to measure the radial runout of the knife shaft and the parallelism of the knife shaft. 5.7.2 Noise test. Use a sound level meter to detect the load noise of the pill making machine according to the provisions of GB/T16769. 5.7.3 Load test.
5.7.3.1 The load test shall be carried out after the idle running test, and the test time shall not be less than 120 minutes. 5.7.3.2 The temperature rise of the transmission box and the reduction box shall be measured with a thermometer. 5.7.3.3 The temperature rise of the bearing shall be measured with a thermometer on the bearing housing. 5.8 Inspection of performance in use
5.8.1 The appearance quality of the pills and the lubricant used shall be visually inspected. 5.8.2 The weight difference of pills shall comply with the provisions of the General Rules for Preparations (Pills) in the Pharmacopoeia of the People's Republic of China (2000 Edition), and the weight difference limit shall be checked according to the second method. If the pills need to be coated with sugar, the weight difference of the pill core shall be checked before coating, and the weight difference shall not be checked after coating.
5.8.3 The qualified rate of pills shall be tested by sampling method: 10 groups of 100 pills are randomly selected from the prepared pills for visual inspection. 5.9 Electrical system safety test method
5.9.1 The continuity, insulation resistance and withstand voltage test of the protective grounding circuit of the electrical system shall be tested according to the provisions of 19.219.3 and 19.4 of GB5226.1-2002 respectively.
5.9.2 The protective grounding circuit, buttons, indicator lights and displays, wiring, markings, warning signs and project codes of the electrical system shall be inspected in accordance with the provisions of 8.2, 10.2, 10.3, Chapter 14 and Chapter 17 of GB5226.1-2002. 6 Inspection rules
The inspection of the pill making machine is divided into factory inspection and type inspection. 6.1 Factory inspection
6.1.1 Before leaving the factory, each pill making machine shall be inspected according to the provisions of Table 1. Only qualified ones are allowed to leave the factory and are accompanied by a product certificate. Table 1 Factory inspection items
Item Category
General items
Main items Date
Inspection items
4.2, 4.3, 4.4.1, 4.4.3, 4.5, 4.6.3, 4.8.2, 4.8.4, 4.8.54.1,4.4.2, 4.6.1,4.6.2, 4.7,4.8.1,4.8.3,4.8.6,4.9, 4.106.1.2 During the inspection process of the pill making machine, if any unqualified items are found, the pill making machine shall be returned for refurbishment and re-inspected after refurbishment. If it still fails to meet the requirements, the product shall be judged as unqualified.
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6.2 Type inspection
6.2.1 Type inspection shall be conducted in any of the following cases: a) When the important structural design, process or material changes of the product may affect the performance and safety of the product; b) When the factory inspection results are significantly different from the last type test; c) When the national quality supervision agency proposes type inspection. 6.2.2 Type inspection items include all the requirements of this standard. JB 20024—2004
6.2.3 Sampling. The type inspection samples shall be selected from the qualified products of the factory inspection according to the method specified in GB/T10111, and one shall be tested.
6.2.4 Judgment rules. In the type inspection, if one of the continuity of the protective grounding circuit, insulation resistance and withstand voltage test in the electrical safety performance fails, the product shall be judged as unqualified in the type inspection. If one of the other items is unqualified, the unqualified item should be retested twice. If it is still unqualified, the product type inspection is deemed unqualified. 7 Marking, instruction manual, packaging, transportation and storage 7.1 Marking
7.1.1 The product label should be fixed at the position specified in the drawing, and the label should comply with the provisions of CB/T13306. The label should include the following contents:
a) Product name and model:
b) Main parameters;
Manufacturer name:
c)
d)
Factory number;
e)
Factory date:
f) Product standard number.
7.1.2
The text and logo on the outer wall of the packaging box should be clear. 7.1.2.1 Storage and transportation marks shall comply with the provisions of GB/T191, including the words or signs "upward", "no paint flipping" 7.1.2.2 Shipping and receiving marks on transport packaging shall comply with the provisions of CB/T6388 and include the following: a) Product name and model;
Shipping date:
b)
Overall dimensions of wooden box;
c
d)
Net weight and gross weight:
e) Name of the shipping and receiving station;
Shipping and receiving Unit.
7.2 Instruction Manual
The product instruction manual shall comply with the provisions of GB/T9969.1 and shall include the following contents: a) Product model and name, manufacturer name, address, zip code and contact number; implemented product standards;
b)
c) Working conditions, power supply, climate environment (such as temperature and humidity, atmospheric pressure, air cleanliness), etc.; d) The main structure, performance, specifications, use, precautions, warnings and prompts, and safety measures of the product;4 Judgment rules. During the type inspection, if any of the electrical safety performance protective grounding circuit continuity, insulation resistance, and withstand voltage tests fails, the product will be judged to have failed the type inspection. If one of the other items is unqualified, the unqualified item should be retested twice. If it is still unqualified, the product will be judged to have failed the type inspection. 7 Logo, instructions for use, packaging, transportation and storage 7.1 Logo
7.1.1 The product should have a product label fixed at the position specified on the drawing, and the label should comply with the regulations of CB/T13306. The sign should include the following content:
a) Product name and model:
b) Main parameters;
Manufacturer name:
c)
d )
factory number;
e)
factory date:
f) product standard number.
7.1.2
The text and markings on the outer wall of the packaging box should be clear. 7.1.2.1 Storage and transportation signs shall comply with the provisions of GB/T191, including the words "upward" and "no turning over paint" or signs. 7.1.2.2 Transportation packaging and receipt signs shall comply with the provisions of CB/T6388, and include the following: a ) Product name, model;
Shipping date:
b)
Wooden box dimensions;
c
d)
Net weight and gross weight:
e) Shipping and receiving station names;
Sending and receiving units.
7.2 Instructions for use
Product instructions for use should comply with GB/T9969. The provisions of .1 should include the following content: a) product model and name, manufacturing unit name, address, postal code and contact number; implemented product standards;
b)
c) working conditions, Power supply, climate environment (such as temperature and humidity, atmospheric pressure, air cleanliness), etc.: d) The main structure, performance, specifications, uses, precautions, warnings and reminder instructions, and safety measures of the product;4 Judgment rules. During the type inspection, if any of the protective grounding circuit continuity, insulation resistance, and withstand voltage tests in the electrical safety performance fails, the product will be judged to have failed the type inspection. If one of the other items is unqualified, the unqualified item should be retested twice. If it is still unqualified, the product will be judged to have failed the type inspection. 7 Logo, instructions for use, packaging, transportation and storage 7.1 Logo
7.1.1 The product should have a product label fixed at the position specified on the drawing, and the label should comply with the regulations of CB/T13306. The sign should include the following content:
a) Product name and model:
b) Main parameters;
Manufacturer name:
c)
d )
factory number;
e)
factory date:
f) product standard number.
7.1.2
The text and markings on the outer wall of the packaging box should be clear. 7.1.2.1 Storage and transportation signs shall comply with the provisions of GB/T191, including the words "upward" and "no turning over paint" or signs. 7.1.2.2 The transportation packaging, receipt and delivery signs shall comply with the provisions of CB/T6388, and include the following: a ) Product name, model;
Shipping date:
b)
Wooden box dimensions;
c
d)bZxz.net
Net weight and gross weight:
e) Shipping and receiving station names;
Sending and receiving units.
7.2 Instructions for use
Product instructions for use should comply with GB/T9969. The provisions of .1 should include the following: a) product model and name, manufacturing unit name, address, postal code and contact number; implemented product standards;
b)
c) working conditions, Power supply, climate environment (such as temperature and humidity, atmospheric pressure, air cleanliness), etc.: d) The main structure, performance, specifications, uses, precautions, warnings and reminder instructions, and safety measures of the product;
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