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Invision 60006022

by Wright Medical Technology, Inc.

Ref 60006022Model 08858251006965UP

Invision 60006022 is a fluted surgical drill bit (EU MDR Class IIa; FDA Class I; FDA product code GFG, Bit, Surgical) made by Wright Medical Technology, Inc., registered in EUDAMED on 13 Oct 2026 (Basic UDI-DI 08858251006965UP) and listed in FDA GUDID since 17 Sep 2016 (UDI-DI 00889797065474), 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 Number08858251006965UP Basic UDI-DI 00889797065474UDI-DIDate13 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00889797065474 UDI-DI Date17 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858251006965UP registered 13 Oct 2026 Active
  • FDA GUDID UDI-DI 00889797065474 listed 17 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00889797065474
  2. Registered EUDAMED 08858251006965UP

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  • Withdrawn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
Invision® EUDAMED
Invision GUDID
Generic name
Fluted surgical drill bit, reusable
Device name
Invision Total Ankle Revision Instruments - Drilling Instrumentation - Class Iia - Non Sterile
Model / Ref / Catalog
60006022, 08858251006965UP
Primary DI / UDI-DI
00889797065474
Basic UDI-DI
08858251006965UP
Direct marketing DI
00889797065474
FDA product code
GFG
EMDN code
L091199 Orthopaedic prosthetics instruments, reusable - other
GMDN term
Fluted surgical drill bit, reusable
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
878.4820
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Outer Diameter — 3.8 Millimeter

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: Fluted surgical drill bit, reusable

Similar devices in this category

Other devices filed under ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER.

Other devices from Wright Medical Technology, Inc.

See all devices from Wright Medical Technology, Inc. →

Properties

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