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Conmed VP8567

by Conmed Corporation

Ref VP8567

Conmed VP8567 is a Class I device made by Conmed Corporation, registered in EUDAMED on 17 Nov 2025 (Basic UDI-DI 084585408516DC) and listed in FDA GUDID since 7 Oct 2021 (UDI-DI 10845854041581), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number084585408516DC Basic UDI-DI 10845854041581UDI-DIDate17 Nov 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number10845854041581 UDI-DI Date7 Oct 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 084585408516DC registered 17 Nov 2025 Active
  • FDA GUDID UDI-DI 10845854041581 listed 7 Oct 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10845854041581
  2. Registered EUDAMED 084585408516DC

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  • Withdrawn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
Conmed
Generic name
Medical device integration rack
Device name
Non-orthopedic, Active, Video Diagnosing/Monitoring, Light source
Model / Ref / Catalog
VP8567
Primary DI / UDI-DI
10845854041581
Basic UDI-DI
084585408516DC
FDA product code
KQM
EMDN code
Z12019099 Various instruments for general and multidisciplinary surgery - other
GMDN term
Medical device integration rack
Device class
Class I
Regulation number
878.4160
EU registration type
Standard device
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution

Related devices

Category: Medical device integration rack

Similar devices in this category

Other devices filed under VARIOUS INSTRUMENTS FOR GENERAL AND MULTIDISCIPLINARY SURGERY - OTHER.

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (21, all answered No)