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DIRECTIVE 2011/65/EU 里面有，不同产品有不同的时间。* A4 ~0 ^/ }5 d( ~. [
3. Paragraph 1 shall apply to medical devices and monitoring and control instruments which are placed on the market from 22 July 2014, to in vitro diagnostic medical devices which are placed on the market from 22 July 2016 and to industrial monitoring and control instruments which are placed on the market from 22 July 2017., H/ G* c3 o$ h( ~! M
4. Paragraph 1 shall not apply to cables or spare parts for the repair, the reuse, the updating of functionalities or upgrading of capacity of the following:
: L1 R2 ^9 n% X9 J6 t2 [(a) EEE placed on the market before 1 July 2006;
I! E1 Z0 n. u6 |- |+ Q4 t(b) medical devices placed on the market before 22 July 2014;
8 g" J9 s4 p3 }* `3 t(c) in vitro diagnostic medical devices placed on the market before 22 July 2016;* Y- R; y% m* O$ j4 u$ K
(d) monitoring and control instruments placed on the market before 22 July 2014;8 N5 e1 S7 }8 g3 ^+ o3 {: y
(e) industrial monitoring and control instruments placed on the market before 22 July 2017;. ]- w" |- ? a/ L; b
(f) EEE which benefited from an exemption and which was placed on the market before that exemption expired as far as that specific exemption is concerned. |
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