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C-Guide-Medium VCG-M

by Versah, LLC

Part of a family of 13 devices: see the family page

Ref VCG-MModel Densah Bur Accessories

C-Guide-Medium VCG-M is a Class I device made by Versah, LLC, registered in EUDAMED on 18 Aug 2026 (Basic UDI-DI 08500176525DENSAH-ACCQ8) and listed in FDA GUDID since 17 Apr 2020 (UDI-DI 00850017652170), 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, GUDID, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08500176525DENSAH-ACCQ8 Basic UDI-DI 00850017652170UDI-DIDate18 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00850017652170 UDI-DI Date17 Apr 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08500176525DENSAH-ACCQ8 registered 18 Aug 2026 Active
  • FDA GUDID UDI-DI 00850017652170 listed 17 Apr 2020 Listed

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Timeline

2 dated events

  1. Listed FDA GUDID 00850017652170
  2. Registered EUDAMED 08500176525DENSAH-ACCQ8

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  • Withdrawn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
Versah C-Guide Sleeve Medium EUDAMED
C-Guide-Medium GUDID
Generic name
Surgical instrument interim-placement holder, reusable
Model / reference
VCG-M, Densah Bur Accessories
Primary DI / UDI-DI
00850017652170
Basic UDI-DI
08500176525DENSAH-ACCQ8
FDA product code
NDP
EMDN code
L159099 Odontostomatology instruments, reusable - other
GMDN term
Surgical instrument interim-placement holder, reusable
Device class
Class I
Regulation number
872.3980
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical instrument interim-placement holder, reusable

Similar devices in this category

Other devices filed under ODONTOSTOMATOLOGY INSTRUMENTS, REUSABLE - OTHER.

Other devices from Versah, LLC

  • Densah Bur Holder VBLK

    Class I

  • VT1525-G

    Class I

  • VT4555-Gs

    Class I

  • VT1525-Gs

    Class I

See all devices from Versah, LLC →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (20, all answered No)