Skip to content

Rebilda Post 1782

by VOCO GmbH

Ref 1782Model posts

Rebilda Post 1782 is a device classified as Class IIa in the EU and Class I in the US made by VOCO GmbH, registered in EUDAMED on 21 Apr 2026 (Basic UDI-DI B-E22117821) and listed in FDA GUDID since 26 Nov 2017 (UDI-DI E22117821), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-E22117821 Basic UDI-DI E22117821UDI-DIDate21 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberE22117821 UDI-DI Date26 Nov 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-E22117821 registered 21 Apr 2026 Active
  • FDA GUDID UDI-DI E22117821 listed 26 Nov 2017 Listed

Timeline

2 dated events

  1. Listed FDA GUDID E22117821
  2. Registered EUDAMED B-E22117821

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  • Withdrawn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
Rebilda Post Set II EUDAMED
Rebilda Post GUDID
Generic name
Dental matrix band, single-use
Model / reference
1782, posts
Primary DI / UDI-DI
E22117821
Basic UDI-DI
B-E22117821
FDA product code
EHQ, KLE, EMA, EBF, ELR, DZA
EMDN code
Z12110180 Instruments for dental treatment units - hardware accessories
GMDN term
Dental matrix band, single-use
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
872.3360, 872.3200, 872.3275, 872.3690, 872.3810, 872.4130
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 I
ImplantableEUDAMED
Yes
GUDID
No

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.

Related devices

Category: Dental composite resinDentine bonding agent/setRoot canal post, preformedDental matrix band, single-use

Similar devices in this category

Other devices filed under INSTRUMENTS FOR DENTAL TREATMENT UNITS - HARDWARE ACCESSORIES.

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)