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DIN EN ISO 10993-1 PDF

DIN EN ISO 10993-1 PDF

Name:
DIN EN ISO 10993-1 PDF

Published Date:
05/01/2021

Status:
Active

Description:

Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2018, including corrected version 2018-10)

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:
Choose Document Language:
$55.59
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File Size : 1 file , 2.8 MB
Note : This product is unavailable in Ukraine, Russia, Belarus
Number of Pages : 52
Product Code(s) : 3260407, 2842664, 3260407, 2842664, 2842664
Published : 05/01/2021

History

DIN EN ISO 10993-1
DIN EN ISO 10993-1
Published Date: 05/01/2021
Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2018, including corrected version 2018-10)
$55.59
DIN EN ISO 10993-1
DIN EN ISO 10993-1
Published Date: 04/01/2010
Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management system (ISO 10993-1:2009)
$41.856
DIN EN ISO 10993-1
DIN EN ISO 10993-1
Published Date: 10/01/2009
Biological evaluation of medical devices - Part 1: Evaluation and testing (ISO 10993-1:2003)
$33.681
DIN EN ISO 10993-1/A1 - DRAFT
DIN EN ISO 10993-1/A1 - DRAFT
Published Date: 03/01/2009
Draft Document - Biological evaluation of medical devices - Part 1: Evaluation and testing (ISO 10993-1:2003); English version FprEN ISO 10993-1:2009, Amendment 1
$13.407
DIN EN ISO 10993-1
DIN EN ISO 10993-1
Published Date: 12/01/2003
Biological evaluation of medical devices - Part 1: Evaluation and testing (ISO 10993-1:2003)
$33.681

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DIN EN ISO 10993-14
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Published Date: 08/01/2009
Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)
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DIN EN ISO 10993-13
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Published Date: 11/01/2010
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010)
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DIN ISO 13022
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Published Date: 06/01/2014
Medical products containing viable human cells - Application of risk management and requirements for processing practices (ISO 13022:2012)
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DIN EN ISO 10993-10
DIN EN ISO 10993-10
Published Date: 04/01/2023
Biological evaluation of medical devices - Part 10: Tests for skin sensitization (ISO 10993-10:2021)
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