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Frc-CK1

by GFAP France

Ref FRC-CK1

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, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number62830879CATAKIT1Z7 Basic UDI-DI 06283087900065UDI-DIDate23 Mar 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
FRC-CK1
Primary DI / UDI-DI
06283087900065
Basic UDI-DI
62830879CATAKIT1Z7
EMDN Code
V9012 Non-specialist surgical instruments and kits, single-use
Device Class
Class I
Medical Purpose
Catakit - disaster kits

Manufacturer details

EUDAMED SRN
FR-PR-000052641

Related devices

Category: Surgical retractor/retraction system blade, single-use

Similar devices

Also classified as Surgical retractor/retraction system blade, single-use.

Other devices from GFAP France

Properties

Other properties (1)

  • Sterile: No