DIN EN ISO 10993-17 PDF

Name:
DIN EN ISO 10993-17 PDF

Published Date:
06/01/2003

Status:
[ Withdrawn ]

Description:

Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)

Publisher:
DIN-adopted European-adopted ISO Standard

Document status:

Active

Format:

Electronic (PDF)

Delivery time:

10 minutes

Delivery time (for Russian version):

200 business days

SKU:

File Size :	1 file
Note :	This product is unavailable in Ukraine, Russia, Belarus
Number of Pages :	30
Product Code(s) :	9516253, 9275670, 9275670, 9516253, 9516253, 9275670
Published :	06/01/2003

History

DIN EN ISO 10993-17

Published Date: 02/01/2024

Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023)

$74.229

DIN EN ISO 10993-17 - DRAFT

Published Date: 12/01/2021

Draft Document - Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO/DIS 10993-17:2021); German and English version prEN ISO 10993-17:2021

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DIN EN ISO 10993-17

Published Date: 08/01/2009

Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002); German version EN ISO 10993-17:2009

$44.472

DIN EN ISO 10993-17

Published Date: 06/01/2003

Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)

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