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Instrument 2200-28g

by Howmedica Osteonics Corp.

Ref 2200-28GModel 08858251005231SU

Instrument 2200-28g is a device classified as Class IIa in the EU and Class II in the US made by Howmedica Osteonics Corp., registered in EUDAMED on 8 Sep 2026 (Basic UDI-DI 08858251005231SU) and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 07613327212884), active as of 24 Oct 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08858251005231SU Basic UDI-DI 07613327212884UDI-DIDate8 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613327212884 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858251005231SU registered 8 Sep 2026 Active
  • FDA GUDID UDI-DI 07613327212884 listed 24 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07613327212884
  2. Registered EUDAMED 08858251005231SU

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  • Withdrawn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
Trident EUDAMED
Instrument GUDID
Generic name
Acetabulum prosthesis trial, prefabricated, reusable
Device name
TF-025 - Class IIa - Hip - Trial Insert
Model / Ref / Catalog
2200-28G, 08858251005231SU
Primary DI / UDI-DI
07613327212884
Basic UDI-DI
08858251005231SU
Direct marketing DI
07613327212884
FDA product code
LPH, LZO, HWC, KWY, MBL, KWL, JDI, KWZ, MAY, MEH, LWJ
EMDN code
V06010101 Hip prostheses testing devices
GMDN term
Acetabulum prosthesis trial, prefabricated, reusable
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
888.3358, 888.3353, 888.3040, 888.3390, 888.3360, 888.3350, 888.3310
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Lumen/Inner Diameter — 28.0 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class II

Related devices

Category: Acetabulum prosthesis trial, prefabricated, reusable

Other devices from Howmedica Osteonics Corp.

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Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Lot / batch number
Other properties (21, all answered No)