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SRPS EN 13795-2:2019

Surgical clothing and drapes - Requirements and test methods - Part 2: Clean air suits

Sep 24, 2019
95.99   Withdrawal of Standard   May 30, 2025

General information

95.99     May 30, 2025

ISS

Z076

European Norm

11.140  

Buying

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Scope

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 manufacturing and processing requirements. This European Standard gives information on the characteristics of single-use and reusable clean air suits used as medical devices for clinical staff, intended to prevent the transmission of infective agents between clinical staff and patients during surgical and other invasive procedures. This European Standard specifies test methods for evaluating the identified characteristics of clean air suits and sets performance requirements for these products.

Related directives

NOTE: If the word "harmonized" (marked in green) is not found in the field with the name of the directive, it means that the European standard is not cited in the OJEU.

93/42/EEC

Medical devices

Harmonized
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

Life cycle

PREVIOUSLY

WITHDRAWN
SRPS EN 13795:2014

NOW

WITHDRAWN
SRPS EN 13795-2:2019
95.99 Withdrawal of Standard
May 30, 2025

REVISED BY

PUBLISHED
SRPS EN 13795-2:2025

Related project

Adopted from EN 13795-2:2019