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CarpoFit®

by implantcast GmbH 10 variants

Ref 00519900Model CARPO18

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4048844CARPO18SD Basic UDI-DI 04048844004026UDI-DIDate30 Jul 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  • Withdrawn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

Model / reference
CARPO18, 00519900
Primary DI / UDI-DI
04048844004026
Basic UDI-DI
4048844CARPO18SD
EMDN code
V0599 Clinical procedures kits not included in other classes - other
Device class
Class IIa
System or procedure pack
Procedure pack
EU registration type
System or procedure pack
Medical purpose
Reusable containers (incl. equipment) are used to contain the instruments required for a specific treatment and to provide a suitable platform for storing surgical instruments during a clinical procedure. They do also serve as protective and transport packaging.

Manufacturer details

EUDAMED SRN
DE-PR-000030803

Other devices from implantcast GmbH

See all devices from implantcast GmbH →

Properties

  • Sterilise before use

Other properties (1)

  • Supplied sterile: No