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Contact Matrix 94272

by Danville Materials, LLC

Ref 94272

Contact Matrix 94272 is a Class I device made by Danville Materials, LLC, registered in EUDAMED on 29 Sep 2026 (Basic UDI-DI 081659402D0202U) and listed in FDA GUDID since 22 Jun 2016 (UDI-DI 00816594022065), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number081659402D0202U Basic UDI-DI 00816594022065UDI-DIDate29 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00816594022065 UDI-DI Date22 Jun 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 081659402D0202U registered 29 Sep 2026 Active
  • FDA GUDID UDI-DI 00816594022065 listed 22 Jun 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00816594022065
  2. Registered EUDAMED 081659402D0202U

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  • Withdrawn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
Contact Matrix
Generic name
Dental matrix band, reusable
Device name
Mega V Matrix System
Model / Ref / Catalog
94272
Primary DI / UDI-DI
00816594022065
Basic UDI-DI
081659402D0202U
FDA product code
EIG
EMDN code
Q01010401 Paper and gutta-percha tips, matrices and wedges for dentistry
GMDN term
Dental matrix band, reusable
Device class
Class I
Regulation number
872.4565
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices in this category

Other devices filed under PAPER AND GUTTA-PERCHA TIPS, MATRICES AND WEDGES FOR DENTISTRY.

Other devices from Danville Materials, LLC

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Properties

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