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请教各位,关于全自动生化分析仪和半自动生化分析仪算IVD指令里的吗?# j7 b* @" x+ c$ o/ p
是不是可以分类到other类里面去?9 c2 Z; z3 c' n! d7 d6 P
如果做CE的话,标准是不是EN 61010-1: 2001 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 1: general requirements 和EN 61326-2-6:2006 Electrical equipment for measurement, control and laboratory use - EMC requirements -- Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment就可以了?' X% }/ x3 ~- {. y; y; R: J4 E1 R1 q
- x+ d- j3 i o7 ~& L需要EN 61010-2-081:2002 Safety requirements for electrical equipment for measurement, control and laboratory use. - Part 2-081: Particular requirements for automatic and semi-automatic laboratory equipment for analysis and other purposes
5 u* E' }, T$ T, S) x* p& DEN 61010-2-101: 2002 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment 吗?
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本来我是把它归到other类里面去的,只需要提供技术文档和符合性声明就可以。; R; C9 v/ K9 l: E
适用标准是:
0 ~/ U3 ], y7 D8 F; O4 K' _) V3 sEN 591:2001 Instructions for use for in vitro diagnostic instruments for professional use % c% @. y8 |; l; y! T6 e& I
EN 980:2003 Graphical symbols for use in the labelling of medical devices
" D. u9 E3 o& y- W% YEN 1658: 1996 Requirements for marking of in vitro diagnostic instruments
/ M' m( f% e* L4 m% p3 DEN 13612:2002 Performance evaluation of in vitro diagnostic medical devices
$ T: |: g0 o6 E/ X+ M1 h: r" KEN 61010-1: 2001 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 1: general requirements , Q) Q+ P7 |2 O% Z0 M$ D% I
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EN 61010-2-081:2002 Safety requirements for electrical equipment for measurement, control and laboratory use. - Part 2-081: Particular requirements for automatic and semi-automatic laboratory equipment for analysis and other purposes; u! K; @# l5 S" ]3 [- M c
. s+ E5 P" ~% l0 i [5 [# OEN 61010-2-101: 2002 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment , f+ B( U$ b/ h2 {1 g# Q: D' P
8 J2 b! E# K d$ X1 d. wEN 61326-2-6:2006 Electrical equipment for measurement, control and laboratory use - EMC requirements -- Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment
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6 m$ P' C1 b9 h( x4 z# ?- _但是前段时间听说,只需要EN 61010-1: 2001和EN 61326-2-6:2006。所以比较困惑了。6 w x* b' n3 d8 j+ j; X. i
盼高手出来解答。谢谢! |
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