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SRPS EN ISO 8637:2014

Cardiovascular implants and extracorporeal systems - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637:2010, including Amendment 1 2013-04-01)

Jul 31, 2014
95.99   Withdrawal of Standard   Oct 30, 2020

General information

95.99     Oct 30, 2020

ISS

Z076

European Norm

11.040.40  

English  

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Scope

ISO 8637:2010 specifies requirements for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators, hereinafter collectively referred to as “the device”, for use in humans.

Related directives

NOTE: If the word "harmonized" (marked in green) is not found in the field with the name of the directive, it means that the European standard is not cited in the OJEU.

93/42/EEC

Medical devices

Life cycle

NOW

WITHDRAWN
SRPS EN ISO 8637:2014
95.99 Withdrawal of Standard
Oct 30, 2020

REVISED BY

WITHDRAWN
SRPS EN ISO 8637-2:2018

PUBLISHED
SRPS EN ISO 8637-1:2020

Related project

Adopted from EN ISO 8637:2014

Adopted from ISO 8637:2010/Amd 1:2013 IDENTICAL

Adopted from ISO 8637:2010 IDENTICAL