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BSI - BS EN ISO 10993-4

Biological evaluation of medical devices Part 4: Selection of tests for interactions with blood

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Organization: BSI
Publication Date: 31 May 2017
Status: active
Page Count: 82
ICS Code (Biological evaluation of medical devices): 11.100.20

Document History

BS EN ISO 10993-4
May 31, 2017
Biological evaluation of medical devices Part 4: Selection of tests for interactions with blood
A description is not available for this item.
BS EN ISO 10993-4
February 28, 2010
Biological evaluation of medical devices Part 4: Selection of tests for interactions with blood
A description is not available for this item.
BS EN ISO 10993-4
November 14, 2002
Biological evaluation of medical devices Part 4: Selection of tests for interactions with blood
A description is not available for this item.
BS EN ISO 10993-4
November 14, 2002
Biological evaluation of medical devices Part 4: Selection of tests for interactions with blood
A description is not available for this item.
BS EN ISO 10993-4
November 14, 2002
Biological evaluation of medical devices Part 4: Selection of tests for interactions with blood
A description is not available for this item.

References

This document references:
BS EN ISO 10993-1 - Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
Published by BSI on December 31, 2020
A description is not available for this item.
This document references:
ISO 10993-1 - Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process
Published by ISO on August 1, 2018
This document specifies: — the general principles governing the biological evaluation of medical devices within a risk management process; — the general categorization of medical devices based on the...
This document references:
ISO 10993-12 FRENCH - Évaluation biologique des dispositifs médicaux — Partie 12: Préparation des échantillons et matériaux de référence
Published by ISO on January 1, 2021
A description is not available for this item.
This document references:
ISO 10993-12 - Biological evaluation of medical devices - Part 12: Sample preparation and reference materials
Published by ISO on January 1, 2021
This document specifies requirements and gives guidance on the procedures in the preparation of samples and the selection of reference materials for medical device testing primarily in biological...
This document references:
3826-1 AMD 1 - Plastics collapsible containers for human blood and blood components — Part 1: Conventional containers AMENDMENT 1
Published by ISO on March 1, 2023
A description is not available for this item.
This document references:
ISO 10993-1 FRENCH - Évaluation biologique des dispositifs médicaux - Partie 1: Évaluation et essais au sein d'un processus de gestion du risque
Published by ISO on August 1, 2018
A description is not available for this item.
This document references:
BS EN ISO 10993-1 - Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
Published by BSI on December 31, 2020
A description is not available for this item.
This document is referenced by:
BS EN ISO 8536-4 - Infusion equipment for medical use Part 4: Infusion sets for single use, gravity feed
Published by BSI on February 29, 2020
A description is not available for this item.
This document is referenced by:
BS EN ISO 1135-4 - Transfusion equipment for medical use Part 4: Transfusion sets for single use, gravity feed
Published by BSI on January 31, 2016
A description is not available for this item.
This document is referenced by:
BS EN ISO 22794 - Dentistry - Implantable materials for bone filling and augmentation in oral and maxillofacial surgery - Contents of a technical file
Published by BSI on September 30, 2009
A description is not available for this item.
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