Greetings,
We are considering refurbishing laboratory equipment products that were
located in the EU. These products will be removed from the EU and
refurbished. Once the products are refurbished, we will be selling them to
new customers in the EU. The refurbishments will not include any "new"
technology. I have a couple of questions for the group in regards to this
process.
1. Will the applicable regulatory requirements of "today" be required,
or the requirements from the original date of sale?
2. Are there any additional requirements for refurbished products?
2. Are there any specific labeling requirements to state that the
product has been refurbished?
3. Are there any type of reporting requirements to let Member States
know that we are performing this refurbishment and reselling the
products in the EU? Would this requirement be different for products
self-certified versus products that required Notified Body Approvals
i.e. Medical, IVD etc.
As always, your responses are appreciated.
Regards
Joe Martin
Applied Biosystems
[email protected]
This message is from the IEEE EMC Society Product Safety
Technical Committee emc-pstc discussion list.
Visit our web site at: http://www.ewh.ieee.org/soc/emcs/pstc/
To cancel your subscription, send mail to:
[email protected]
with the single line:
unsubscribe emc-pstc
For help, send mail to the list administrators:
Ron Pickard: [email protected]
Dave Heald: [email protected]
For policy questions, send mail to:
Richard Nute: [email protected]
Jim Bacher: [email protected]
Archive is being moved, we will announce when it is back on-line.
All emc-pstc postings are archived and searchable on the web at:
http://www.ieeecommunities.org/emc-pstc
