BB/T 0059-2012 in English

VALID

Co-extrusion films for the vaccum thermoforming packaging of medical devices

Issued on:2012-05-24
Implemented on:2012-11-01
File Format:PDF
Delivery:Via email within 1~3 business days

Price(USD)： $180.00
$175.00

Standard No:	BB/T 0059-2012
Document status:	VALID
Title in English:	Co-extrusion films for the vaccum thermoforming packaging of medical devices
Title in Chinese:	医疗器械吸塑包装用共挤膜
Language:	English
File Format:	Electronic (PDF)
Delivery:	Via email within 1~3 business days
Issued on:	2012-05-24
Implemented on:	2012-11-01
ICS Classification:	55.040-Packaging materials and accessories
Chinese Classification:	A82-Packaging material and container
Professional Classification:	BB-Packaging
Related Keywords:	medical devices medical devices introductionthis standard medical device packaging materials co-extrusion films multi-layer co-extrusion film
Related Topics:	medical plastic What does a class of medical devices include? medical suction cup What does a class of medical devices include? military medical kit Medical devices include What are the second class medical devices? doctor pack What are the second class medical devices? Medical Device Packaging Regulations Primary packaging requirements for medical devices Medical Device Packaging Regulations Class I Medical Device Packaging Requirements For pharmaceutical plastic packaging Class I medical device packaging Class I device packaging Medical device packaging size Medical device hollow packaging Quality assessment of medical device plastic parts Bioburden requirements for inner packaging of medical devices Which medical device noise is applicable? Medical plastic packaging Medical device packaging design Medical+filter membrane bag+ Medical device testing UV absorbance bb/t 0060 Packaging film parameters

本标准规定了医疗器械吸塑包装用共挤膜的产品分类、要求、试验方法、检验规则和标志、包装、运输、贮存。
本标准适用于以聚丙烯（PP）、聚酰胺（PA）和聚乙烯（PE）为原料，按不同结构采用共挤出工艺形成的膜。
本标准不适用于人体植入性医疗器械。

Introduction

This standard outlines the specifications for a type of multi-layer co-extrusion film used in vacuum packaging for medical devices. It covers the material composition, physical properties, and testing methods required to ensure the film meets the necessary quality and performance criteria. The document provides detailed requirements for production, inspection, and acceptance procedures. It also includes guidelines for labeling and packaging practices to ensure product safety and effectiveness. The standard is applicable to manufacturers, suppliers, and users of medical device packaging materials. It serves as a reference for ensuring consistency and reliability in the production and use of such packaging materials.

*** Please note: This description may not be accurate, please refer to the official documentation.

More samples: YD/T 3934-2021 DL/T 5154-2012 DL/T 368-2010

Sample only — not a preview of BB/T 0059-2012