Standard [WITHDRAWN]
Product information on this site:
Quick delivery via download or delivery service
All transactions are encrypted
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. This document has been prepared by CEN/TC 205 "Non-active medical devices", the secretariat of which is held by DIN (Germany). The responsible German Committee is NA 063-01-08 GA "Operationstextilien" ("Surgical textiles") at the Medical Standards Committee and the Textiles and Textile Machinery Standards Committee.
This document replaces DIN EN 13795-1:2009-10 , DIN EN 13795-2:2009-12 , DIN EN 13795-3:2009-12 .
This document has been replaced by: DIN EN 13795-1:2019-06 , DIN EN 13795-2:2019-06 , DIN EN 13795:2013-10 .