Norm

NEN-EN 13795:2011+A1:2013 en

Chirurgisch afdekmateriaal, operatiejassen en clean air suits, gebruikt als medische hulpmiddelen voor patienten, klinisch personeel en apparatuur - Algemene eisen voor fabrikanten, bewerkers en producten, beproevingsmethoden, prestatie-eisen en prestatie-niveaus

49,30

Over deze norm

Status Definitief
Aantal pagina's 22
Commissie OK-jassen en afdekmaterialen
Gepubliceerd op 01-02-2013
Taal Engels
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.

Details

ICS-code 11.140
Nederlandse titel Chirurgisch afdekmateriaal, operatiejassen en clean air suits, gebruikt als medische hulpmiddelen voor patienten, klinisch personeel en apparatuur - Algemene eisen voor fabrikanten, bewerkers en producten, beproevingsmethoden, prestatie-eisen en prestatie-niveaus
Engelse titel 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
Vervangt
Normatieve verwijzingen
  • 93/42/EEG, Medische hulpmiddelen

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