ГОСТ РЕН 14254—2010
Библиография
[
1
]
EN 37S
[
2
]
EN 550
[
3
]
EN 552
И]
EN 554
Information supplied by manufacturer with in vitrodiagnostic reagents for professional use
Sterilization of medical devices — Validation androutine control of ethylene oxide stenllzation
Stenllzation of medical devices — Validation androutine control of sterilizing by Irradiation
Sterilization of medical devices — Validation androutine control of sterilization by moist heat
15]
EN 829
In vitro diagnostic systems — Transport packages for medical and biological speciments —
Requirements, tests
Graphical symbols for use in the labeling of medical devices
Information supplied by manufacturer with medical devices
Single-use containers for human venous blood specimen collection
[
6
]
EN 980
(7)
EN 1041
18]
EN 14820
[9]
ISO 7000
Graphical symbols for use on equipment — Index and synopsis
[
10
]
ISO 15223
Medical devices — Symbols to be used with medical device labels, labeling and information to be
supplied
Dangerous Goods Regulations — Packing Instruction 602
[
11
]
UN 602
[
12
]
UN 650
Dangerous Goods Regulations — Packing Instruction 650
[13] CouncilDirective of27 June 1967 on the approximationoflaws, regulations and administrative provisions relating tothe
classification, packaging and labeling of dangerous substances (67/548/EEC). OJ. 1967. N» 1. 196
[14] Council Directive 93M2/EEC of 14 June 1993 concerning medical devices OJ. 1993. № 1. 169
[15]
Directive 98/79IEC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical
devices. 1998. № L 331.
14