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Valor 4150004030

by Wright Medical Technology, Inc.

Ref 4150004030Model 08858251006919UG

Valor 4150004030 is a device classified as Class IIa in the EU and Class I in the US made by Wright Medical Technology, Inc., registered in EUDAMED on 12 Oct 2026 (Basic UDI-DI 08858251006919UG) and listed in FDA GUDID since 17 Sep 2016 (UDI-DI 00889797061407), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08858251006919UG Basic UDI-DI 00889797061407UDI-DIDate12 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00889797061407 UDI-DI Date17 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858251006919UG registered 12 Oct 2026 Active
  • FDA GUDID UDI-DI 00889797061407 listed 17 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00889797061407
  2. Registered EUDAMED 08858251006919UG

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  • Withdrawn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
Valor® EUDAMED
Valor GUDID
Generic name
Orthopaedic guidewire, reusable
Device name
VALOR INSTRUMENTATION - GUIDE-WIRES, K-WIRES, PINS - CLASS lla - STERILE
Model / Ref / Catalog
4150004030, 08858251006919UG
Primary DI / UDI-DI
00889797061407
Basic UDI-DI
08858251006919UG
FDA product code
FZX
EMDN code
P09120301 Kirschner bone wires
GMDN term
Orthopaedic guidewire, reusable
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
878.4800
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class I

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Orthopaedic guidewire, reusable

Similar devices

Also classified as Orthopaedic guidewire, reusable.

Similar devices in this category

Other devices filed under BONE FIXATION WIRES.

Other devices from Wright Medical Technology, Inc.

See all devices from Wright Medical Technology, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction)
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (17, all answered No)