Skip to content

Structur 2 1312

by VOCO GmbH

Ref 1312

Structur 2 1312 is a device classified as Class IIa in the EU and Class II in the US made by VOCO GmbH, registered in EUDAMED on 30 Mar 2026 (Basic UDI-DI ++E2210425010000000DP) and listed in FDA GUDID since 31 Aug 2016 (UDI-DI E22113121), 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++E2210425010000000DP Basic UDI-DI E22113121UDI-DIDate30 Mar 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberE22113121 UDI-DI Date31 Aug 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI ++E2210425010000000DP registered 30 Mar 2026 Active
  • FDA GUDID UDI-DI E22113121 listed 31 Aug 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID E22113121
  2. Registered EUDAMED ++E2210425010000000DP

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  • Withdrawn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
Structur 2
Generic name
Temporary dental crown/bridge
Model / Ref / Catalog
1312
Primary DI / UDI-DI
E22113121
Basic UDI-DI
++E2210425010000000DP
FDA product code
EBG
EMDN code
Q01020605 Temporary dental prostheses
GMDN term
Temporary dental crown/bridge
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
872.3770
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.

Similar devices in this category

Other devices filed under TEMPORARY DENTAL PROSTHESES.

Other devices from VOCO GmbH

See all devices from VOCO GmbH →

Properties

  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (22, all answered No)