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6250-45-25

by Zimmer, Inc.

Ref 00-6250-045-25

6250-45-25 (00-6250-045-25) is a device classified as Class IIb in the EU and Class II in the US made by Zimmer, Inc., registered in EUDAMED on 2 Nov 2026 (Basic UDI-DI B-00889024119734) and listed in FDA GUDID since 24 Nov 2017 (UDI-DI 00889024119734), 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-00889024119734 Basic UDI-DI 00889024119734UDI-DIDate2 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00889024119734 UDI-DI Date24 Nov 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00889024119734 registered 2 Nov 2026 Active
  • FDA GUDID UDI-DI 00889024119734 listed 24 Nov 2017 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00889024119734
  2. Registered EUDAMED B-00889024119734

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  • Withdrawn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

Generic name
Revision uncoated hip femur prosthesis
Device name
HP Acetabular Screws_ BONE SCREW 4.5 Implants
Model / Ref / Catalog
00-6250-045-25, 6250-45-25
Primary DI / UDI-DI
00889024119734
Basic UDI-DI
B-00889024119734
FDA product code
LPH
EMDN code
P09088099 Hip prostheses - other accessories
GMDN term
Revision uncoated hip femur prosthesis
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
888.3358
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Size
Length — 25 Millimeter

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
00-6250-045-25
GUDID
6250-45-25
Device classEUDAMED
Class IIb
GUDID
Class II

Device class is stated on each registry's own scale: Class IIb 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: Revision uncoated hip femur prosthesis

Similar devices in this category

Other devices filed under HIP PROSTHESES - OTHER ACCESSORIES.

Other devices from Zimmer, Inc.

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Properties

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