Skip to content

V-Print DT 6908

by VOCO GmbH

Ref 6908

V-Print DT 6908 is a device classified as Class IIa in the EU and Class II in the US made by VOCO GmbH, registered in EUDAMED on 11 Sep 2026 (Basic UDI-DI ++E2210491140000000KC) and listed in FDA GUDID since 6 Dec 2023 (UDI-DI E22169081), 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 Number++E2210491140000000KC Basic UDI-DI E22169081UDI-DIDate11 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberE22169081 UDI-DI Date6 Dec 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI ++E2210491140000000KC registered 11 Sep 2026 Active
  • FDA GUDID UDI-DI E22169081 listed 6 Dec 2023 Listed

Timeline

2 dated events

  1. Listed FDA GUDID E22169081
  2. Registered EUDAMED ++E2210491140000000KC

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  • Withdrawn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
V-Print DT
Generic name
Resin artificial teeth
Model / Ref / Catalog
6908
Primary DI / UDI-DI
E22169081
Basic UDI-DI
++E2210491140000000KC
FDA product code
ELM
EMDN code
Q01020605 Temporary dental prostheses
GMDN term
Resin artificial teeth
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
872.3590
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class II

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

Related devices

Category: Resin artificial teeth

Similar devices in this category

Other devices filed under TEMPORARY DENTAL PROSTHESES.

Other devices from VOCO GmbH

See all devices from VOCO GmbH →

Properties

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