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Tri a

by Tri Dental Implants Int. AG 24 variants

Part of a family of 23 devices: see the family page

Ref MUA-IMPR

Tri a (MUA-IMPR) is a Class I device made by Tri Dental Implants Int. AG, registered in EUDAMED on 1 Sep 2026 (Basic UDI-DI 764014988IMPRKC) and listed in FDA GUDID since 15 Apr 2024 (UDI-DI 07640149887082), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number764014988IMPRKC Basic UDI-DI 07640149887082UDI-DIDate1 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07640149887082 UDI-DI Date15 Apr 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 764014988IMPRKC registered 1 Sep 2026 Active
  • FDA GUDID UDI-DI 07640149887082 listed 15 Apr 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07640149887082
  2. Registered EUDAMED 764014988IMPRKC

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  • Withdrawn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
Tri
Generic name
Dental implant system
Device name
Impression posts
Model / Ref / Catalog
MUA-IMPR, A
Primary DI / UDI-DI
07640149887082
Basic UDI-DI
764014988IMPRKC
FDA product code
NDP
EMDN code
P01020180 Dental implants - accessories
GMDN term
Dental implant system
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
MRI safety
MR Conditional

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
MUA-IMPR
GUDID
A
ImplantableEUDAMED
No
GUDID
Yes

Related devices

Category: Dental implant system

Similar devices in this category

Other devices filed under DENTAL IMPLANTS - ACCESSORIES.

Other devices from Tri Dental Implants Int. AG

See all devices from Tri Dental Implants Int. AG →

Properties

  • Sterilise before use
  • Single use
  • Implantable NoEUDAMEDYesGUDID
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (18, all answered No)