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ISO 9073-11

Textiles Test methods for nonwovens Part 11: Run-off

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Organization: ISO
Publication Date: 1 November 2002
Status: active
Page Count: 16
ICS Code (Textile fabrics): 59.080.30

Document History

ISO 9073-11
November 1, 2002
Textiles Test methods for nonwovens Part 11: Run-off
A description is not available for this item.

References

This document is referenced by:
EN 13795 - Surgical drapes, gowns and clean air suits, used as medical devices for patients, clinical staff and equipment - General requirements for manufacturers, processors and products, test methods, performance requirements and performance levels
Published by CEN on March 1, 2011
This European Standard specifies information to be supplied to users and third party verifiers in addition to the usual labelling of medical devices (see EN 980 and EN 1041), concerning manufacturing...
This document is referenced by:
DIN EN 13795 - Surgical drapes, gowns and clean air suits, used as medical devices for patients, clinical staff and equipment - General requirements for manufacturers, processors and products, test methods, performance requirements and performance levels; German version EN 13795:2011+A1:2013
Published by DIN on October 1, 2013
Diese Europäische Norm legt die Informationen fest, die dem Anwender und Prüfer (Dritte) zu liefern sind, zusätzlich zu der normalen Kennzeichnung von Medizinprodukten (siehe EN 980 und EN 1041)...
This document is referenced by:
EN 13795-1 - Surgical clothing and drapes - Requirements and test methods - Part 1: Surgical drapes and gowns
Published by CEN on April 1, 2019
This document specifies information to be supplied to users and third party verifiers in addition to the usual labelling of medical devices (see EN 1041 and EN ISO 15223-1), concerning manufacturing...
This document is referenced by:
SN EN 13795-1 - Surgical clothing and drapes - Requirements and test methods - Part 1: Surgical drapes and gowns
Published by SNV on November 1, 2019
This European Standard specifies information to be supplied to users and third party verifiers in addition to the usual labelling of medical devices (see EN 1041 and EN ISO 15223-1), concerning...
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