G
Gargi
Hello Everyone,
I have got this issue related to my ongoing work.
Is there a need to provide justification to the concerned authoriy/communicate with end user(i.e customer) ,that the components used are RoHS 2 and REACh compliant.?
If yes , what is the appropriate way to do so.
If not, then how shall I prove that device is RoHS/REACh compliant.
Kindly provide your valueable anwers!!
Help is appreciated!!
I have got this issue related to my ongoing work.
- The scenario is as below:
- A medical device manufactured in Europe.
- It is not CE marked
- Now the company wants the device to be RoHS 2 compliant before 22nd july 2014.
Is there a need to provide justification to the concerned authoriy/communicate with end user(i.e customer) ,that the components used are RoHS 2 and REACh compliant.?
If yes , what is the appropriate way to do so.
If not, then how shall I prove that device is RoHS/REACh compliant.
Kindly provide your valueable anwers!!
Help is appreciated!!