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V-Print SG 6131

by VOCO GmbH

Ref 6131

V-Print SG 6131 is a device classified as Class IIa in the EU and Class I in the US made by VOCO GmbH, registered in EUDAMED on 30 Mar 2026 (Basic UDI-DI ++E2210491020000000HF) and listed in FDA GUDID since 1 Jul 2020 (UDI-DI E22161311), active as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number++E2210491020000000HF Basic UDI-DI E22161311UDI-DIDate30 Mar 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberE22161311 UDI-DI Date1 Jul 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI ++E2210491020000000HF registered 30 Mar 2026 Active
  • FDA GUDID UDI-DI E22161311 listed 1 Jul 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID E22161311
  2. Registered EUDAMED ++E2210491020000000HF

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  • Withdrawn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 SG
Generic name
Dental guided surgery reference plate
Model / Ref / Catalog
6131
Primary DI / UDI-DI
E22161311
Basic UDI-DI
++E2210491020000000HF
FDA product code
KMY
EMDN code
Q010399 Surgical dental devices - other
GMDN term
Dental guided surgery reference plate
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
872.5525
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 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.

Similar devices in this category

Other devices filed under SURGICAL DENTAL DEVICES - OTHER.

Other devices from VOCO GmbH

See all devices from VOCO GmbH →

Properties

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