Just checking to make sure I understand.
For Europe the 60601-1 medical standard transitions from 2nd to 3rd edition. It
does the same in the US next June.
So after June 1s we can't ship to the EU but
What about products that are in our customers warehouses in the EU at
that time? Do they have to be recalled or can they be used until the warehouse
is empty?
They are in EU but can they cross boarders?
We are just looking at our inventory split. We have completed the 60601-2 3rd
edition for the products being currently produced, but the customer has some
volume of them in EU in their possession. As those are depleted their stocks
will be current edition units will be shipped to fill the inventory.
They haven't mentioned anything about them just yet, but I'm trying to
anticipate the question.
Thanks
Gary McInturff
Reliability/Compliance Engineer
Esterline Interface Technologies
Featuring
ADVANCED INPUT, MEMTRON, and LRE MEDICAL products
600 W. Wilbur Avenue
Coeur d'Alene, ID 83815-9496
Office:208-635-8306
Cell: 509 868 2279
Toll Free: 800-444-5923 X 1238
gary.mcintu...@esterline.com<mailto:brian.s...@esterline.com>
www.esterline.com/interfacetechnologies<http://www.esterline.com/advancedinput>
Technology, Innovation, Performance...
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