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Scanabutment 3.03.778

by Thommen Medical AG

Part of a family of 77 devices: see the family page

Ref 3.03.778

Scanabutment 3.03.778 is a Class I device made by Thommen Medical AG, registered in EUDAMED on 20 Mar 2026 (Basic UDI-DI 7640156473501032211235YC) and listed in FDA GUDID since 13 Jul 2020 (UDI-DI 07640156478402), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number7640156473501032211235YC Basic UDI-DI 07640156478402UDI-DIDate20 Mar 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07640156478402 UDI-DI Date13 Jul 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 7640156473501032211235YC registered 20 Mar 2026 Active
  • FDA GUDID UDI-DI 07640156478402 listed 13 Jul 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07640156478402
  2. Registered EUDAMED 7640156473501032211235YC

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  • Withdrawn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
Scanabutment
Generic name
Radiographic image marker, manual
Device name
Prosthetic
Model / reference
3.03.778
Primary DI / UDI-DI
07640156478402
Basic UDI-DI
7640156473501032211235YC
FDA product code
NDP
EMDN code
P01020180 Dental implants - accessories
GMDN term
Radiographic image marker, manual
Device class
Class I
Regulation number
872.3980
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Radiographic image marker, manual

Similar devices in this category

Other devices filed under DENTAL IMPLANTS - ACCESSORIES.

Other devices from Thommen Medical AG

See all devices from Thommen Medical AG →

Properties

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