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SSH EN 13795:2011+A1:2013

Veshje kirurgjikale, veshjet dhe kostumet me ajër të cilat përdoren si pajisje mjekësore për pacientët, stafin e klinikës dhe pajisjet - Kërkesa të përgjithshme për fabrikuesit, procesorët dhe produktet, metodat e provës; kërkesat e performancës dhe nivelet e performancës

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
27 nën 2013

General information

60.60     27 nën 2013

DPS

DPS/KT 316

European Norm

11.140  

anglisht  

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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 980 and EN 1041), concerning manufacturing and processing requirements. This European Standard gives information on the characteristics of single-use and reusable surgical gowns, surgical drapes and clean air suits used as medical devices for patients, clinical staff and equipment, intended to prevent the transmission of infective agents between patients and clinical staff during surgical and other invasive procedures. This European Standard specifies test methods for evaluating the identified characteristics of surgical drapes, gowns and clean air suits and sets performance requirements for these products.
EN 13795 does not cover requirements for flammability of products. Suitable test methods for flammability and resistance to penetration by laser radiation, together with an appropriate classification system, are given in EN ISO 11810-1 and EN ISO 11810-2. Additional essential requirements that apply to surgical clothing and drapes are covered by other European Standards.

Related directives

Directives related to this standards.

93/42/EEC

Pajisje Mjekësore

2007/47/EC

Direktiva 2007/47/EC e Parlamentit Europian dhe e Këshillit të 5 shtator 2007 amendon Direktivën e Këshillit 90/385/EEC mbi përafrimin e ligjeve të Shteteve Anëtare në lidhje me pajisje medicinale aktive transplatuese, Direktiva e Këshillit 93/42/EEC në lidhje me pajisjet mjekësore dhe Direktivën 98/8/EC në lidhje me vendosjen e produkteve biocide në treg

Life cycle

NOW

PUBLISHED
SSH EN 13795:2011+A1:2013
60.60 Standard published
27 nën 2013

Related project

Adopted from EN 13795:2011+A1:2013

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