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Bone Management MI193

by Hager & Meisinger Gesellschaft mit beschränkter Haftung

Ref MI193Model Surgical hand-held instruments

Bone Management MI193 is a Class I device made by Hager & Meisinger Gesellschaft mit beschränkter Haftung, registered in EUDAMED on 19 Mar 2025 (Basic UDI-DI ++E0HM209I04ABPW) and listed in FDA GUDID since 4 Jun 2025 (UDI-DI E0HM39MI1931), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID NumberE0HM39MI1931 UDI-DI Date4 Jun 2025ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number++E0HM209I04ABPW Basic UDI-DI E0HM39MI1931UDI-DIDate19 Mar 2025RegisteredStatusActive

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI ++E0HM209I04ABPW registered 19 Mar 2025 Active
  • FDA GUDID UDI-DI E0HM39MI1931 listed 4 Jun 2025 Listed

Timeline

2 dated events

  1. Registered EUDAMED ++E0HM209I04ABPW
  2. Listed FDA GUDID E0HM39MI1931

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  • Withdrawn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
Bone Management
Generic name
Periotome, reusable
Model / Ref / Catalog
MI193, Surgical hand-held instruments
Primary DI / UDI-DI
E0HM39MI1931
Basic UDI-DI
++E0HM209I04ABPW
FDA product code
DZN
EMDN code
Q0199 Odontology devices - other
GMDN term
Periotome, reusable
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

Related devices

Category: Periotome, reusable

Similar devices in this category

Other devices filed under ODONTOLOGY DEVICES - OTHER.

Other devices from Hager & Meisinger Gesellschaft mit beschränkter Haftung

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Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (19, all answered No)