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JB/T 20099-2022 English PDF

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JB/T 20099-2022: Pharmaceutical agitated nutsche filter dryer
Status: Valid

JB/T 20099: Historical versions

Standard IDUSDBUY PDFLead-DaysStandard Title (Description)Status
JB/T 20099-2022259 Add to Cart 3 days Pharmaceutical agitated nutsche filter dryer Valid
JB/T 20099-2007599 Add to Cart 3 days Drug filter washing dryer Obsolete

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GB/T 36030   JB/T 20032   JB/T 20104   JB/T 20100   JB/T 20106   JB/T 20098   

Basic data

Standard ID: JB/T 20099-2022 (JB/T20099-2022)
Description (Translated English): Pharmaceutical agitated nutsche filter dryer
Sector / Industry: Mechanical & Machinery Industry Standard (Recommended)
Classification of Chinese Standard: C92
Classification of International Standard: 11.120.30
Word Count Estimation: 11,121
Date of Issue: 2022-04-24
Date of Implementation: 2022-10-01
Older Standard (superseded by this standard): JB/T 20099-2007
Issuing agency(ies): Ministry of Industry and Information Technology
Summary: This standard specifies the classification and types, requirements, test methods, inspection rules and signs, instructions for use, packaging, transportation and storage of pharmaceutical filtration, washing and drying machine products. This standard applies to pharmaceutical filtration washing and drying machines.

JB/T 20099-2022: Pharmaceutical agitated nutsche filter dryer

---This is a DRAFT version for illustration, not a final translation. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.) will be manually/carefully translated upon your order.
Pharmaceutical agitated nutsche filter dryer ICS 11.120.30 CCSC92 Record number. 86933-2022 Machinery Industry Standard of the People's Republic of China Replacing JB/T 20099-2007 Drug filter washing and drying machine Released on 2022-04-24 2022-10-01 implementation Released by the Ministry of Industry and Information Technology of the People's Republic of China Published by China Standard Press

table of contents

Preface I 1 Scope 1 2 Normative references 1 3 Terms and Definitions 1 4 Classification and Model 2 4.1 Classification 2 4.2 Model 2 5 requirements 2 5.1 Design and manufacture 2 5.2 Materials 2 5.3 Appearance 2 5.4 Performance 2 5.5 Electrical system safety 3 5.6 Drug filtration washing dry mass 3 6 Test method 3 6.1 Performance test 3 6.2 Drug filtration, washing and drying quality test 4 7 Inspection rules 5 7.1 Inspection classification 5 7.2 Factory inspection 5 7.3 Type inspection 5 8 Signs, instructions for use, packaging, transportation and storage 6 8.1 Flag 6 8.2 Instruction Manual 6 8.3 Packaging 6 8.4 Transport 6 8.5 Storage 6 Appendix A (Normative) Preparation process for samples using calcium gluconate 7

foreword

This document is in accordance with the provisions of GB/T 1.1-2020 "Guidelines for Standardization Work Part 1.Structure and Drafting Rules for Standardization Documents" drafting. This document replaces JB/T 20099-2007 "Drug Filtration Washing and Drying Machine". Compared with JB/T 20099-2007, this standard except for the structure In addition to adjustments and editorial changes, the main technical changes are as follows. --- Changed the terms and definitions (see 3.1, 3.1 of the.2007 edition); --- Changed the model number (see 4.2, 4.2 of the.2007 edition); --- Changed the design and manufacturing requirements (see 5.1, 5.1 of the.2007 edition); --- Changed the material requirements (see 5.2, 5.2 of the.2007 edition); --- Increased safety interlock (see 5.4.8, 5.4.9); --- Increase the safety clearance between the stirring paddle and the mesh surface and cylinder wall (see 5.4.10); --- Changed the quality of the filter washing and drying machine (see 5.6, 5.6 of the.2007 edition); --- Changed the performance test (see 6.1, 6.4 of the.2007 edition); ---Deleted the remaining powder cake thickness (5.4.9 of the.2007 edition); --- Deleted Appendix B (see Appendix B of the.2007 edition). This document is proposed by China Pharmaceutical Equipment Industry Association. This document is under the jurisdiction of the National Pharmaceutical Equipment Standardization Technical Committee (SAC/TC356). This document is drafted by. Zhejiang Yaguang Technology Co., Ltd. The main drafters of this document. Xin Dandan, He Minghong, Lin Baokang, Lin Peigao, Han Yunsheng. This document was first released in.2007, and this is the first revision. Drug filter washing and drying machine

1 Scope

This document specifies the classification and model, requirements, test methods, inspection rules, signs, and instructions for use of pharmaceutical filter washing and drying machines. Books, packaging, transport and storage. This document applies to pharmaceutical filter washing and drying machines (hereinafter referred to as three-in-one).

2 Normative references

The contents of the following documents constitute the essential provisions of this document through normative references in the text. Among them, dated references For documents, only the version corresponding to the date is applicable to this document; for undated reference documents, the latest version (including all amendments) is applicable to this document. GB/T 150.1~150.4 Pressure vessels GB/T 191 Packaging, storage and transportation icon marks GB/T 3768 Acoustic sound pressure method for measuring sound power level and sound energy level of noise sources adopts the simple method of enveloping the measuring surface above the reflecting surface. easy method GB/T 4272 General Rules for Equipment and Pipeline Insulation Technology GB/T 6388 Transport packaging receipt and delivery marks GB 8599 Technical Requirements for Large Steam Sterilizer Automatic Control Type GB/T 9969 General Rules for Instructions for Use of Industrial Products GB/T 10111 Generation of Random Numbers and Its Application in Product Quality Sampling Inspection GB/T 13306 Signage GB/T 13384 General Technical Specifications for Packaging of Mechanical and Electrical Products GB/T 36030 General Technical Requirements for Cleaning in Place and Sterilization of Pharmaceutical Machinery (Equipment) GB/T 36035 General Requirements for Electrical Safety of Pharmaceutical Machinery JB/T 20188-2017 Pharmaceutical machinery product model compilation method NB/T 10558 Pressure vessel coating and transport packaging TSG21 Safety Technical Supervision Regulations for Stationary Pressure Vessels Pharmacopoeia of the People's Republic of China (2020 Edition)

3 Terms and Definitions

The following terms and definitions apply to this document. 3.1 It is a multi-functional machine that keeps the materials in the same container in a sealed manner and continuously completes the process operations of filtering, washing, drying, and automatic discharging (dissolving and discharging).
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