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DIN EN ISO 20696

Sterile urethral catheters for single use (ISO 20696:2018, Corrected version 2019-12)

active, Most Current
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Organization: DIN
Publication Date: 1 October 2020
Status: active
Page Count: 42
ICS Code (Syringes, needles and catheters): 11.040.25

Document History

DIN EN ISO 20696
October 1, 2020
Sterile urethral catheters for single use (ISO 20696:2018, Corrected version 2019-12)
A description is not available for this item.
DIN EN ISO 20696
April 1, 2019
Sterile urethral catheters for single use (ISO 20696:2018, Corrected version 2018-09)
A description is not available for this item.
DIN EN ISO 20696
October 1, 2018
Sterile urethral catheters for single use (ISO 20696:2018)
This document specifies requirements and test methods for sterile urethral catheters for single use, with or without a balloon. This document does not include drainage catheters covered by ISO 20697,...
DIN EN ISO 20696
March 1, 2017
Sterile urethal catheters for single use (ISO/DIS 20696:2017); German and English version prEN ISO 20696:2017
This standard specifies requirements and test methods for sterile urethral catheters for single use, with or without a balloon. This standard does not include drainage catheters covered by ISO 20697...

References

This document references:
15223-1 - Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements
Published by ISO on July 1, 2021
This document specifies symbols used to express information supplied for a medical device. This document is applicable to symbols used in a broad spectrum of medical devices, that are available...
This document references:
ISO 10993-2 - Biological evaluation of medical devices Part 2: Animal welfare requirements
Published by ISO on July 15, 2006
This part of ISO 10993 is aimed at those who commission, design and perform tests or evaluate data from animal tests undertaken to assess the biocompatibility of materials intended for use in medical...
This document references:
ISO 10993-3 - Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity
Published by ISO on October 1, 2014
This part of ISO 10993 specifies strategies for risk estimation, selection of hazard identification tests and risk management, with respect to the possibility of the following potentially...
This document references:
ISO 10993-5 - Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity
Published by ISO on June 1, 2009
This part of ISO 10993 describes test methods to assess the in vitro cytotoxicity of medical devices. These methods specify the incubation of cultured cells in contact with a device and/or extracts...
This document references:
ISO 10993-7 - Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals
Published by ISO on October 15, 2008
This part of ISO 10993 specifies allowable limits for residual ethylene oxide (EO) and ethylene chlorohydrin (ECH) in individual EO-sterilized medical devices, procedures for the measurement of EO...
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