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TorqLine™ Handpiece adapter

by Adin Dental Implant Systems LTD.

Ref RA1002Model Tool

TorqLine™ Handpiece adapter (RA1002) is a Class I device made by Adin Dental Implant Systems Ltd., registered in EUDAMED on 7 May 2026 (Basic UDI-DI 729011677TorqWrenchAdapBT) and listed in FDA GUDID since 18 Dec 2025 (UDI-DI 07290116778457), 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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number729011677TorqWrenchAdapBT Basic UDI-DI 07290116778457UDI-DIDate7 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07290116778457 UDI-DI Date18 Dec 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 729011677TorqWrenchAdapBT registered 7 May 2026 Active
  • FDA GUDID UDI-DI 07290116778457 listed 18 Dec 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07290116778457
  2. Registered EUDAMED 729011677TorqWrenchAdapBT

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  • Withdrawn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

Generic name
Dental torque wrench adaptor
Model / reference
Tool, RA1002
Primary DI / UDI-DI
07290116778457
Basic UDI-DI
729011677TorqWrenchAdapBT
FDA product code
NDP
EMDN code
L0317 General surgery adapters and connectors, reusable
GMDN term
Dental torque wrench adaptor
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

Manufacturer details

EUDAMED SRN
IL-MF-000014625
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

Similar devices in this category

Other devices filed under GENERAL SURGERY ADAPTERS AND CONNECTORS, REUSABLE.

Other devices from Adin Dental Implant Systems Ltd.

See all devices from Adin Dental Implant Systems Ltd. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (20, all answered No)