SN/T 0323.3-2007 English PDF

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SN/T 0323.3-2007: Rules for the inspection of medical equipment for import and export. Part 3: Plastics collapsible containers for human blood. Blood components conventional containers
Status: Valid

Standard ID	USD	BUY PDF	Lead-Days	Standard Title (Description)	Status
SN/T 0323.3-2007	259	Add to Cart	3 days	Rules for the inspection of medical equipment for import and export. Part 3: Plastics collapsible containers for human blood. Blood components conventional containers	Valid

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Basic data

Standard ID: SN/T 0323.3-2007 (SN/T0323.3-2007)
Description (Translated English): Rules for the inspection of medical equipment for import and export. Part 3: Plastics collapsible containers for human blood. Blood components conventional containers
Sector / Industry: Commodity Inspection Standard (Recommended)
Classification of Chinese Standard: C48
Classification of International Standard: 11.040.20
Word Count Estimation: 8,875
Date of Issue: 2007-12-24
Date of Implementation: 2008-07-01
Older Standard (superseded by this standard): SN/T 0964-2000
Quoted Standard: GB/T 2828.1; GB 14232.1-2004; SN/T 0002; YY 0466; Chinese Pharmacopoeia (2005 edition)
Regulation (derived from): ?Industry Standard Filing Announcement 2008 No.2 (Total No.98)
Issuing agency(ies): General Administration of Customs
Summary: This standard specifies the import and export of conventional blood bag sampling, testing and conformity determination. This standard applies to a closed, sterile row or even traditional blood bags, the bags can bring blood collection, blood transfusion jack, lancets and the transfer tube. According to requirements, blood bags can be loaded anticoagulants and (or) maintenance solution.

SN/T 0323.3-2007: Rules for the inspection of medical equipment for import and export. Part 3: Plastics collapsible containers for human blood. Blood components conventional containers

---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.
Rules for the inspection of medical equipment for import and export Part 3. Plastics collapsible containers for human blood Blood components conventional containers. Exit inspection and quarantine industry standard book People's Republic of China Instead of the SN/T 0964-2000 Inspection of import and export of medical devices Part 3. human blood and blood components Bag Conventional plastic container bags Posted 2007-12-24 2008-07-01 implementation People's Republic of China The State Administration of Quality Supervision, Inspection and Quarantine released

Foreword

SN/T 0323 "Importers of medical equipment for the inspection," is divided into three parts. --- Part 1. one-time infusion (blood) control; --- Part 2. a one-time use of sterile syringes; --- Part 3. human blood and blood components bag plastic containers conventional blood bag. This section SN/T Section 30323 of. The partial replacement of SN/T 0964-2000 "Importers disposable plastic bags for the inspection." This section compared with the SN/T 0964-2000 The main changes are as follows. --- Technical requirements and test methods used in the ISO 3826-1.2003 international standard; --- Term corresponds with international standards; --- Modify the scope of regulations; --- Inspection of the product name was changed to conventional disposable plastic bags by the blood bag; --- In the chemical requirements to remove the "zinc", adding "metal, color, ammonium ions and alcohol effluent" inspection requirements; --- Removed in the biological requirements "mold, blood storage test, acute systemic toxicity," added "microbial impermeability, cytotoxic "Of testing and require the sterilization process control for each batch sterilization validation reports and batch quality records; --- In the physical requirements to remove the "seal blood bags, transfer bags airtight, eccentric resistance, temperature resistance, water vapor permeability, sticky labels Even firmness, "increased" thermal stability, resistance to leakage, revealing vapor, particulate pollution "inspection requirements; --- Increased imports conformity assessment models; --- Increase unpacking inspection test mode. Appendix A of this section is an informative annex. This section proposed and managed by the National Certification and Accreditation Administration Committee. This section was drafted by. People's Republic of China Exit Inspection and Quarantine of Jilin, Jilin Medical Device Testing. The main drafters of this section. Caizhao Hong, Zhang Jingping, Song Yongli, Wu Ping, Hou Wan Ling, He Zhonghui. This part of the standard replaces the previous editions are. --- SN/T 0964-2000. Inspection of import and export of medical devices Part 3. human blood and blood components Bag Conventional plastic container bags

1 Scope

SN/T 0323 provisions of this part of the sampling, testing and qualification of import and export of traditional bags judgment. This section applies to a closed, sterile row or even conventional blood bag (hereinafter referred to as "blood bags"), which can bring blood collection bags, blood transfusion jack, Lancets and transfer tube. According to requirements, anticoagulants and blood bags can be loaded (or) maintenance solution.

2 Normative references

The following documents contain provisions which, through reference SN/T 0323 this section, constitute provisions of this part. For dated reference documents Member, all subsequent amendments (not including errata content) or revisions do not apply to this section, however, encouraged to reach under this section Parties to research agreement to use the latest versions of these documents. For undated reference documents, the latest versions apply to this section. GB/T 2828.1 Sampling procedures for inspection - Part 1. by acceptance quality limit (AQL) retrieval batch inspection sampling plan (ISO 2859-1.1999, IDT) GB 14232.1-2004 human blood and blood components bag plastic containers - Part 1. Conventional blood bags (ISO 3826-1. 2003, IDT) The basic provisions of SN/T 0002 Electromechanical Import and Export Commodity Inspection procedures prepared Symbol YY0466 medical equipment used with medical device labels, labeling and information provided People's Republic of China Pharmacopoeia (2005 edition)

3 Terms and Definitions

GB/T 2828.1, SN/T 0002 and established the following terms and definitions apply to SN/T 0323 of this section. 3.1 According to a predetermined cycle based on national technical specifications mandatory requirements, type testing, according to the scene to examine the provisions of the product or batch Pumping batch sampling, determination and implementation of qualified supervision activities of the enterprise quality management system. 3.2 Mandatory requirements by national technical specifications, by checking the technical documentation and the necessary by-batch or batch sampling pump, for goods Compliance Judgment and evaluation activities. 3.3 When imported goods at the port of entry in accordance with relevant state regulations for goods related files, documents, technical data and goods mainly conducted Inspection activities. 3.4 For the implementation of sampling and collection of the same specifications, models, produced under the same conditions of production per unit of product, referred to as batch. ......

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