NF EN 1283

NF EN 1283

June 1996
Standard Cancelled

Haemodialysers, haemodiafilters, haemofilters, haemoconcentrators and their extracorporeal circuits.

Le présent document détermine les méthodes pour la vérification des caractéristiques physiques et biologiques des hémodialyseurs, hémodiafiltres, hémofiltres, hémoconcentrateurs et circuits extracorporels.

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Collections

National standards and national normative documents

Publication date

June 1996

Number of pages

22 p.

Reference

NF EN 1283

ICS Codes

11.040.20   Transfusion, infusion and injection equipment
11.040.60   Therapy equipment

Classification index

S93-302

Print number

1 - 01/06/1996

European kinship

EN 1283:1996
Sumary
Haemodialysers, haemodiafilters, haemofilters, haemoconcentrators and their extracorporeal circuits.

Le présent document détermine les méthodes pour la vérification des caractéristiques physiques et biologiques des hémodialyseurs, hémodiafiltres, hémofiltres, hémoconcentrateurs et circuits extracorporels.
Replaced standards (1)
NF S90-302
February 1990
Standard Cancelled
Medico-surgical equipment. Single-use, sterile haemodialysers haemodiafilters and haemofilters.

La présente norme fait partie d'un ensemble de normes traitant du matériel de dialyse (synonyme : appareil d'épuration extra-rénale) : raccords et lignes de dialyse, générateurs, moniteurs-distributeurs de dialyse péritonéale,... La présente norme a pour objet d'établir les spécifications relatives aux appareils non réutilisables et stériles conçus pour réaliser l'hémodialyse, l'hémodiafiltration et l'hémofiltration chez l'homme. Elle précise les méthodes de référence permettant de vérifier ces spécifications. La présente norme sert de base à l'homologation des hémodialyseurs, des hémodiafiltres et des hémofiltres, délivrée par le Ministère chargé de la Santé.

Standard replaced by (2)
NF EN ISO 8638
March 2014
Standard Cancelled
Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters

ISO 8638:2010 specifies requirements for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (hereafter referred to as “the device”) and (integral and non-integral) transducer protectors which are intended for use in haemodialysis, haemodiafiltration and haemofiltration.

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.

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