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Biomet® Hip System 163663

by Biomet Orthopedics, Inc.

Ref 163663

Biomet® Hip System 163663 is a device classified as Class III in the EU and Class II in the US made by Biomet Orthopedics, Inc., registered in EUDAMED on 31 Oct 2026 (Basic UDI-DI B-00887868308284) and listed in FDA GUDID since 18 Apr 2019 (UDI-DI 00887868308284), 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-00887868308284 Basic UDI-DI 00887868308284UDI-DIDate31 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00887868308284 UDI-DI Date18 Apr 2019ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00887868308284 registered 31 Oct 2026 Active
  • FDA GUDID UDI-DI 00887868308284 listed 18 Apr 2019 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00887868308284
  2. Registered EUDAMED B-00887868308284

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  • Withdrawn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
Biomet® Hip System
Generic name
Metallic femoral head prosthesis
Device name
HP Ringloc CoCr Type 1
Model / Ref / Catalog
163663
Primary DI / UDI-DI
00887868308284
Basic UDI-DI
B-00887868308284
FDA product code
LPH, LZO, JDI, KRO, JDG
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
888.3358, 888.3353, 888.3350, 888.3510, 888.3360
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands
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 Biomet Orthopedics, Inc.

See all devices from Biomet Orthopedics, Inc. →

Properties

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