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Meron Plus 1732

by VOCO GmbH

Ref 1732Model liquid

Meron Plus 1732 is a device classified as Class IIa in the EU and Class II in the US made by VOCO GmbH, registered in EUDAMED on 22 Apr 2026 (Basic UDI-DI B-E22117321) and listed in FDA GUDID since 31 Aug 2016 (UDI-DI E22117321), active as of 22 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDD

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/MDD EUDAMED NumberB-E22117321 Basic UDI-DI E22117321UDI-DIDate22 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberE22117321 UDI-DI Date31 Aug 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-E22117321 registered 22 Apr 2026 Active
  • FDA GUDID UDI-DI E22117321 listed 31 Aug 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID E22117321
  2. Registered EUDAMED B-E22117321

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Meron Plus
Generic name
Dental composite resin
Model / Ref / Catalog
1732, liquid
Description
Resin reinforced glass ionomer luting cement. Liquid 10 ml.
Primary DI / UDI-DI
E22117321
Basic UDI-DI
B-E22117321
FDA product code
EMA
EMDN code
Q0101010299 Temporary and permanent dental restoration cements - other
GMDN term
Dental composite resin
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
872.3275
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class II
ImplantableEUDAMED
Yes
GUDID
No

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: Dental composite resin

Similar devices in this category

Other devices filed under TEMPORARY AND PERMANENT DENTAL RESTORATION CEMENTS - OTHER.

Other devices from VOCO GmbH

See all devices from VOCO GmbH →

Properties

  • Implantable YesEUDAMEDNoGUDID
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (19, all answered No)