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Instrument 1090-3258

by Howmedica Osteonics Corp.

Ref 1090-3258Model 08858251005229T9

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

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08858251005229T9 Basic UDI-DI 07613327244762UDI-DIDate12 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613327244762 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

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  • Withdrawn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 - Constrained Liner Trial
Model / Ref / Catalog
1090-3258, 08858251005229T9
Primary DI / UDI-DI
07613327244762
Basic UDI-DI
08858251005229T9
Direct Marketing DI
07613327244762
FDA Product Code
KWY, LWJ, HWC, LZO, MBL, MAY, JDI, KWL, KWZ, MEH, LPH
EMDN Code
V06010101 Hip prostheses testing devices
GMDN Term
Acetabulum prosthesis trial, prefabricated, reusable
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
888.3390, 888.3360, 888.3040, 888.3353, 888.3358, 888.3350, 888.3310
Market of Registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

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.

See all devices from Howmedica Osteonics Corp. →

Properties

  • Reusable
  • Prescription Use
  • Lot / Batch Number

Other properties (21)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No