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Bullet Nose 475823

by Biomet Orthopedics, Inc.

Part of a family of 9 devices: see the family page

Ref 475823

Bullet Nose 475823 is a Class I device made by Biomet Orthopedics, Inc., registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI 889024AXY4C) and listed in FDA GUDID since 2 Apr 2022 (UDI-DI 00887868508134), active as of 7 Nov 2026.

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

CE MDR

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/MDR EUDAMED Number889024AXY4C Basic UDI-DI 00887868508134UDI-DIDate29 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00887868508134 UDI-DI Date2 Apr 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 889024AXY4C registered 29 Oct 2026 Active
  • FDA GUDID UDI-DI 00887868508134 listed 2 Apr 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00887868508134
  2. Registered EUDAMED 889024AXY4C

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
Bullet Nose
Generic name
Acetabular orthopaedic reamer
Device name
Comprehensive SRS Cylindrical Reamers
Model / Ref / Catalog
475823
Primary DI / UDI-DI
00887868508134
Basic UDI-DI
889024AXY4C
FDA product code
HTO
EMDN code
L091102 Orthopaedic prostheses reamers and burs, reusable
GMDN term
Acetabular orthopaedic reamer
Device class
Class I
Regulation number
888.4540
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Acetabular orthopaedic reamer

Similar devices in this category

Other devices filed under ORTHOPAEDIC PROSTHESES REAMERS AND BURS, REUSABLE.

Other devices from Biomet Orthopedics, Inc.

See all devices from Biomet Orthopedics, Inc. →

Properties

  • Sterilise before use
  • Reusable
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction)
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (19, all answered No)