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Instrument 2200-44I

by Howmedica Osteonics Corp.

Ref 2200-44IModel 08858251005231SU

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08858251005231SU Basic UDI-DI 07613327244410UDI-DIDate8 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613327244410 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  • Withdrawn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 - Trial Insert
Model / Ref / Catalog
2200-44I, 08858251005231SU
Primary DI / UDI-DI
07613327244410
Basic UDI-DI
08858251005231SU
Direct Marketing DI
07613327244410
FDA Product Code
KWL, MAY, LPH, MEH, MBL, LWJ, JDI, KWY, LZO, HWC, KWZ
EMDN Code
V06010101 Hip prostheses testing devices
GMDN Term
Acetabulum prosthesis trial, prefabricated, reusable
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
888.3360, 888.3353, 888.3358, 888.3350, 888.3390, 888.3040, 888.3310
Market of Registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization
Size
Lumen/Inner Diameter — 44.0 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.

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