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HM236 020

by Hager & Meisinger Gesellschaft mit beschränkter Haftung

HM236 020 (500106001291020) is a Class I device made by Hager & Meisinger Gesellschaft mit beschränkter Haftung, listed in FDA GUDID since 15 Sep 2021 (UDI-DI E0HM29002361060201), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberE0HM29002361060201 UDI-DI Date15 Sep 2021ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name
Metal/carbide ENT bur, reusable
Model / Ref / Catalog
HM236 020, 500106001291020
Primary DI / UDI-DI
E0HM29002361060201
FDA product code
EJL
GMDN term
Metal/carbide ENT bur, reusable
Device class
Class I
Regulation number
872.3240
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Metal/carbide ENT bur, reusable

Other devices from Hager & Meisinger Gesellschaft mit beschränkter Haftung

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)