PacificMark Notified Body
VerifiedNotified Body for medical devices (MDR/IVDR).
Certification Body
Testing Laboratory
UKAS·17065DAkkS·17025
About
EU Notified Body 2854. MDR and IVDR conformity assessments, plus UKCA and FDA 510(k) submissions.
What we do
- MDR Annex IX & X
- 510(k) US agent service
- UKCA + CE in one engagement
Standards & schemes
Industries served
Medical Devices
Electronics
Regions covered
EU
UK
USA
Reviews & ratings
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