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Evonos 26-000008

by evonos GmbH & Co. KG

Evonos 26-000008 is a Class II device made by evonos GmbH & Co. KG, listed in FDA GUDID since 25 Apr 2024 (UDI-DI 04054462020959), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04054462020959 UDI-DI Date25 Apr 2024ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Evonos
Generic name
Automatic cranial perforator, single-use
Model / reference
26-000008
Primary DI / UDI-DI
04054462020959
FDA product code
HBF
GMDN term
Automatic cranial perforator, single-use
Device class
Class II
Regulation number
882.4305
GUDID distribution status
In Commercial Distribution

Related devices

Category: Automatic cranial perforator, single-use

Other devices from evonos GmbH & Co. KG

See all devices from evonos GmbH & Co. KG →

Properties

  • Supplied sterile
  • Single use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)