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EN ISO 10555-1:2013

Intravascular catheters - Sterile and single-use catheters - Part 1: General requirements (ISO 10555-1:2013, Corrected version 2014-01-15) EN ISO 10555-1:2013

Publication date:   Aug 15, 2013

General information

99.60 Withdrawal effective   Nov 29, 2023

CEN

CEN/TC 205 Non-active medical devices

European Norm

11.040.25   Syringes, needles and catheters

Buying

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Scope

ISO 10555-1:2013 specifies general requirements for intravascular catheters, supplied in the sterile condition and intended for single use, for any application.

Related legislation

Legislation related to this standard

93/42/EEC

Medical devices

Legislation 93/42/EEC
2007/47/EC

Directive 2007/47/EC of the European Parliament and of the council of 5 September 2007 amending Council Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices, Council Directive 93/42/EEC concerning medical devices and Directive 98/8/EC concerning the placing of biocidal products on the market

Legislation 2007/47/EC

Life cycle

PREVIOUSLY

WITHDRAWN
EN ISO 10555-2:1997/AC:2002

WITHDRAWN
EN ISO 10555-1:2009

WITHDRAWN
EN ISO 10555-2:1997

NOW

WITHDRAWN
EN ISO 10555-1:2013
99.60 Withdrawal effective
Nov 29, 2023

CORRIGENDA / AMENDMENTS

WITHDRAWN
EN ISO 10555-1:2013/A1:2017

REVISED BY

PUBLISHED
EN ISO 10555-1:2023