ASTM-F2475 Historical Revision Information
Biocampatability Evaluation of Medical Device Packaging Materials, Standard Guide For

ASTM-F2475 - 2011 EDITION - SUPERSEDED
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Standard Guide for Biocompatibility Evaluation of Medical Device Packaging Materials
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Scope

1.1 This guide provides information to determine the appropriate testing for biocompatibility of materials (or packaging materials) in sterile barrier systems used to contain a medical device.

1.2 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and to determine the applicability of regulatory limitations prior to use.

Significance and Use

The compatibility of packaging materials with a medical device is a requirement of many regulatory bodies. Since most medical devices are used or implanted in, around or on the human body, these devices must do no harm. Therefore, the packaging materials that come in contact with the medical device must also be evaluated and determined to be safe for use with the human body in that they have no negative impact on the physical, chemical or biological properties of the device. . This evaluation may include both a study of relevant experience with and actual testing of packaging materials. Such an evaluation may result in the conclusion that no testing is needed if the material has a demonstrable history of safe use in the specific role that is the same as that of the package under design.

The medical device manufacturer determines the need for appropriate testing, with consideration of the device/package interactions, if any. The responsibility of the packaging supplier is typically limited to the performance of cytotoxicity testing.

Keywords

biocompatibility; cytotoxicity; medical device; medical device packaging; toxicity; Biocompatibility; Cytotoxicity; Medical devices/equipment; Medical/surgical packaging materials; Toxicity/toxicology

To find similar documents by ASTM Volume:

15.10 (Packaging; Flexible Barrier Packaging)

To find similar documents by classification:

11.120.99 (Other standards related to pharmaceutics Including equipment for pharmaceutical industry)

55.020 (Packaging and distribution of goods in general)

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Document Number

ASTM-F2475-11

Revision Level

2011 EDITION

Status

Superseded

Modification Type

Revision

Publication Date

April 1, 2011

Document Type

Guide

Page Count

4 pages

Committee Number

F02.15