SN/T 3062.4-2011 in English

VALID

Packing Materials for Terminally Sterilized Medical Devices for Import. Part 4: Requirements for Materials and Sterile Barrier Systems of Importing Medical Device Sterilization Packaging

Issued on:2011-09-09
Implemented on:2012-04-01
File Format:PDF
Delivery:Via email within 1~3 business days

Price(USD)： $240.00
$233.00

Standard No:	SN/T 3062.4-2011
Document status:	VALID
Title in English:	Packing Materials for Terminally Sterilized Medical Devices for Import. Part 4: Requirements for Materials and Sterile Barrier Systems of Importing Medical Device Sterilization Packaging
Title in Chinese:	进口医疗器械灭菌包装第4部分：材料和预成型无菌屏障系统要求
Language:	English
File Format:	Electronic (PDF)
Delivery:	Via email within 1~3 business days
Issued on:	2011-09-09
Implemented on:	2012-04-01
Professional Classification:	SN-Import&Export Inspection
Related Keywords:	medical device sterilization packaging materials importing medical device sterilization packaging scopethis part sterile barrier systems sterilization packaging materials terminally sterilized medical devices
Related Topics:	sterile sterile barrier system barrier system Imported medical devices Import of medical equipment Aseptic system sterile english Test Methods for Sterile Medical Device Packaging Part 18 Import of medical equipment Imported medical devices New Pharmaceutical Packaging Materials Class I Medical Device Packaging Requirements Sterilization packaging Sterility requirements Porous Material Packaging Barrier Systems Sterilization and bandaging method for wide-mouth bottles Sterile instrument package weight Medical device sterilization packaging standards and requirements

Scope

This part of SN/T 3062 specifies the requirements and testing methods for sterilization packaging materials and preformed sterile barrier systems for imported medical devices. This section applies to the inspection of imported medical device sterilization packaging materials and preformed sterile barrier systems. This section does not include requirements for drug/device combinations and quality assurance systems for production control at each stage of the sterile barrier system.

More samples: QC/T 942-2021 DL/T 368-2010 GB 18306-2015

Sample only — not a preview of SN/T 3062.4-2011

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