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Namic

by Medline International France 196 variants

Ref NANK60002

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3666520DCNAMICsystemsSTUU Basic UDI-DI 03666520157401UDI-DIDate16 Sep 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
NAMIC Systems sterile
Model / Reference
NANK60002
Primary DI / UDI-DI
03666520157401
Basic UDI-DI
3666520DCNAMICsystemsSTUU
EMDN Code
C01040199 Cardiac angiography devices - other
Device Class
Class IIa
Medical Purpose
For Angiography procedure

Manufacturer details

EUDAMED SRN
FR-PR-000003713

Other devices from Medline International France

See all devices from Medline International France →

Properties

  • Sterile