K
Kiera
Hello,
I am looking for information on how to acquire a device listing from FDA (if necessary) to support the export of a CE-marked Class IIa device which is as of yet uncleared by FDA.
FDA guidance on the topic indicates the need for a device listing (without which I am concerned the devices will not clear customs), but EU does not require a Certificate of Exportability, so I am not sure how to go about acquiring a listing number.
I welcome any suggestions/guidance.
Thanks,
K
I am looking for information on how to acquire a device listing from FDA (if necessary) to support the export of a CE-marked Class IIa device which is as of yet uncleared by FDA.
FDA guidance on the topic indicates the need for a device listing (without which I am concerned the devices will not clear customs), but EU does not require a Certificate of Exportability, so I am not sure how to go about acquiring a listing number.
I welcome any suggestions/guidance.
Thanks,
K