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Oktagon® 72089

by Hager & Meisinger Gesellschaft mit beschränkter Haftung

Part of a family of 63 devices: see the family page

Ref 72089Model Accessories implantology and oral surgery

Oktagon 72089 is a manual non-rotary dental instrument handle (EU MDR Class I; FDA Class I; FDA product code DZN, Instruments, Dental Hand) made by Hager & Meisinger Gesellschaft mit beschränkter Haftung, registered in EUDAMED on 19 May 2025 (Basic UDI-DI ++E0HM351I05AAPZ) and listed in FDA GUDID since 15 Sep 2021 (UDI-DI E0HM720891), 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 Number++E0HM351I05AAPZ Basic UDI-DI E0HM720891UDI-DIDate19 May 2025RegisteredStatusActive
United StatesGUDID listing GUDID NumberE0HM720891 UDI-DI Date15 Sep 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI ++E0HM351I05AAPZ registered 19 May 2025 Active
  • FDA GUDID UDI-DI E0HM720891 listed 15 Sep 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID E0HM720891
  2. Registered EUDAMED ++E0HM351I05AAPZ

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  • Withdrawn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
Oktagon EUDAMED
Oktagon® GUDID
Generic name
Manual non-rotary dental instrument handle
Model / Ref / Catalog
72089, Accessories implantology and oral surgery
Primary DI / UDI-DI
E0HM720891
Basic UDI-DI
++E0HM351I05AAPZ
FDA product code
DZN
EMDN code
Q0199 Odontology devices - other
GMDN term
Manual non-rotary dental instrument handle
Device class
Class I
Regulation number
872.4565
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

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Other devices filed under ODONTOLOGY DEVICES - OTHER.

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (21, all answered No)