SS-EN-ISO-10555-1 › Intravascular catheters - Sterile and single-use catheters - Part 1: General requirements (ISO 10555-1:2013, Corrected version 2013-07-01)

SS-EN-ISO-10555-1 - 2013 EDITION - CURRENT
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Included in this current edition are the following subparts:

 2013 EDITION - Aug. 9, 2013
 FOR 2013 EDITION AMENDMENT 1 SEE SS-EN-ISO-10555-1-AM1 - Dec. 20, 2017

This part of ISO 10555 specifies general requirements for intravascular catheters, supplied in the sterile condition and intended for single use, for any application.lt is not applicable to intravascular catheter accessories, e.g. those covered by ISO 11070.

To find similar documents by classification:

11.040.20 (Transfusion, infusion and injection equipment Including blood packs Syringes, needles and catheters, see 11.040.25)

11.040.25 (Syringes, needles and catheters)


Medical devices. 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

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Designation Name

SS-EN ISO 10555-1:2013

Revision Level

2013 EDITION

Status

Current

Publication Date

Aug. 9, 2013

Language(s)

English

Page Count

40

International Equivalent

EN ISO 10555-1:2013(IDT); ISO 10555-1:2013(IDT)