Ovaj deo standarda utvrđuje zahteve i metode ispitivanja za materijale, sterilne pregradne sisteme i ambalažne sisteme koji su namenjeni za održavanje sterilnosti terminalno sterilisanih medicinskih sredstava do momenta upotrebe.
Директиве повезане са овим стандардом
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
ПОВУЧЕН
SRPS EN ISO 11607-1:2017
95.99
Повучен
22. 6. 2020.
ОБЈАВЉЕН
SRPS EN ISO 11607-1:2020