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Friadent® 32451620

by Dentsply Implants Manufacturing GmbH

Ref 45-1620

Friadent® 32451620 (45-1620) is a device classified as Class IIa in the EU and Class II in the US made by Dentsply Implants Manufacturing GmbH, registered in EUDAMED on 3 Nov 2026 (Basic UDI-DI B-07392532227493) and listed in FDA GUDID since 18 Nov 2020 (UDI-DI 07392532227493), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-07392532227493 Basic UDI-DI 07392532227493UDI-DIDate3 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07392532227493 UDI-DI Date18 Nov 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-07392532227493 registered 3 Nov 2026 Active
  • FDA GUDID UDI-DI 07392532227493 listed 18 Nov 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07392532227493
  2. Registered EUDAMED B-07392532227493

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  • Withdrawn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
FRIADENT® Transfer Coping Transfer Technique D3.0/GH3 EUDAMED
Friadent® GUDID
Generic name
Dental implant suprastructure, temporary, preformed, single-use
Model / Ref / Catalog
45-1620, 32451620
Primary DI / UDI-DI
07392532227493
Basic UDI-DI
B-07392532227493
FDA product code
DZE
EMDN code
P01020180 Dental implants - accessories
GMDN term
Dental implant suprastructure, temporary, preformed, single-use
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
872.3640
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 3 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
45-1620
GUDID
32451620
Device classEUDAMED
Class IIa
GUDID
Class II
ImplantableEUDAMED
No
GUDID
Yes

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Dental implant suprastructure, temporary, preformed, single-use

Similar devices in this category

Other devices filed under DENTAL IMPLANTS - ACCESSORIES.

Other devices from Dentsply Implants Manufacturing GmbH

See all devices from Dentsply Implants Manufacturing GmbH →

Properties

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