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Try-in Screw Trefoil™ 3/pkg

by Nobel Biocare AB 2 variants

Ref 300082

Try-in Screw Trefoil™ 3/pkg (300082) is a Class I device made by Nobel Biocare AB, registered in EUDAMED on 8 Dec 2025 (Basic UDI-DI 733274700000020772) and listed in FDA GUDID since 16 May 2025 (UDI-DI 07332747213317), active as of 22 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number733274700000020772 Basic UDI-DI 07332747213317UDI-DIDate8 Dec 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number07332747213317 UDI-DI Date16 May 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 733274700000020772 registered 8 Dec 2025 Active
  • FDA GUDID UDI-DI 07332747213317 listed 16 May 2025 Listed

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Timeline

2 dated events

  1. Listed FDA GUDID 07332747213317
  2. Registered EUDAMED 733274700000020772

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  • Withdrawn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
Try-in Screw Trefoil™ 3/pkg EUDAMED
Trefoil™ GUDID
Generic name
Dental implant suprastructure, temporary, preformed, single-use
Device name
Trefoil lab tools for prosthetics
Model / Ref / Catalog
300082
Primary DI / UDI-DI
07332747213317
Basic UDI-DI
733274700000020772
Unit of use DI
07332747154894
FDA product code
NDP
EMDN code
Q010299 Prosthetic dentistry devices - other
GMDN term
Dental implant suprastructure, temporary, preformed, single-use
Device class
Class I
Regulation number
872.3980
EU registration type
Standard device
EU market of registration
Sweden
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
ImplantableEUDAMED
No
GUDID
Yes

Manufacturer details

EUDAMED SRN
SE-MF-000000009

Similar devices in this category

Other devices filed under DEVICES FOR PROSTHETIC DENTISTRY.

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Properties

  • Single use
  • Implantable NoEUDAMEDYesGUDID
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (19, all answered No)