Skip to content

ic-head CoCrMo taper 12/14 23872815

by implantcast GmbH

Ref 23872815Model ICHEADCOCRUNC

ic-head CoCrMo taper 12/14 23872815 is a device classified as Class III in the EU and Class II in the US made by implantcast GmbH, registered in EUDAMED on 6 Nov 2026 (Basic UDI-DI B-04048844017071) and listed in FDA GUDID since 1 Oct 2020 (UDI-DI 04048844017071), active as of 7 Nov 2026.

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-04048844017071 Basic UDI-DI 04048844017071UDI-DIDate6 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04048844017071 UDI-DI Date1 Oct 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04048844017071 registered 6 Nov 2026 Active
  • FDA GUDID UDI-DI 04048844017071 listed 1 Oct 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04048844017071
  2. Registered EUDAMED B-04048844017071

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
ic-head CoCrMo taper 12/14
Generic name
Metallic femoral head prosthesis
Model / reference
23872815, ICHEADCOCRUNC
Primary DI / UDI-DI
04048844017071
Basic UDI-DI
B-04048844017071
FDA product code
KWY
EMDN code
P090804050202 Metal femoral heads, total hip replacement
GMDN term
Metallic femoral head prosthesis
Device class
Class III EUDAMED
Class II GUDID
Regulation number
888.3390
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class III
GUDID
Class II

Device class is stated on each registry's own scale: Class III in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Metallic femoral head prosthesis

Similar devices in this category

Other devices filed under METAL FEMORAL HEADS, TOTAL HIP REPLACEMENT.

Other devices from implantcast GmbH

See all devices from implantcast GmbH →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (19, all answered No)