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Axiom® INMD075

by Etablissements Anthogyr

Ref INMD075Model Extractor instrument (Torque transmission)

Axiom® INMD075 is a Class I device made by Etablissements Anthogyr, registered in EUDAMED on 20 May 2026 (Basic UDI-DI 36633940054QZ) and listed in FDA GUDID since 20 Dec 2023 (UDI-DI 03663394482844), 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 Number36633940054QZ Basic UDI-DI 03663394482844UDI-DIDate20 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number03663394482844 UDI-DI Date20 Dec 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 36633940054QZ registered 20 May 2026 Active
  • FDA GUDID UDI-DI 03663394482844 listed 20 Dec 2023 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 03663394482844
  2. Registered EUDAMED 36633940054QZ

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  • Withdrawn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
Axiom EUDAMED
Axiom® GUDID
Generic name
Screw extractor, reusable
Model / reference
INMD075, Extractor instrument (Torque transmission)
Primary DI / UDI-DI
03663394482844
Basic UDI-DI
36633940054QZ
FDA product code
NDP
EMDN code
Q010299 Prosthetic dentistry devices - other
GMDN term
Screw extractor, reusable
Device class
Class I
Regulation number
872.3980
EU registration type
Standard device
EU market of registration
France
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Screw extractor, reusable

Similar devices in this category

Other devices filed under PROSTHETIC DENTISTRY DEVICES - OTHER.

Other devices from Etablissements Anthogyr

See all devices from Etablissements Anthogyr →

Properties

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