NF EN ISO 8637-2

NF EN ISO 8637-2

August 2018
Standard Cancelled

Extracorporeal systems for blood purification — Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters

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Main informations

Collections

National standards and national normative documents

Publication date

August 2018

Number of pages

30 p.

Reference

NF EN ISO 8637-2

ICS Codes

11.040.20   Transfusion, infusion and injection equipment
11.040.60   Therapy equipment

Print number

1

International kinship

ISO 8637-2:2018

European kinship

EN ISO 8637-2:2018
Replaced standards (1)
NF EN ISO 8637
March 2014
Standard Cancelled
Cardiovascular implants and extracorporeal systems - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators

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

Standard replaced by (1)
NF EN ISO 8637-2
April 2024
Standard Current
Extracorporeal systems for blood purification - Part 2 : extracorporeal blood and fluid circuits for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators

This document specifies requirements for disposable extracorporeal blood and fluid circuits and accessories used in combination with haemodialysis equipment intended for extracorporeal blood treatment therapies such as, but not limited to, haemodialysis, haemodiafiltration, haemofiltration. This document does not apply to: ?     haemodialysers, haemodiafilters or haemofilters; ?     plasmafilters; ?     haemoperfusion devices; ?     vascular access devices. NOTE 1        Requirements for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators are specified in ISO 8637-1. NOTE 2        Requirements for plasmafilters are specified in ISO 8637-3.

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