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debritom+ 2000.0200

by Medaxis AG 2 variants

debritom+ 2000.0200 is a Class II device made by Medaxis AG, listed in FDA GUDID since 3 Apr 2019 (UDI-DI B724200002000), not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 NumberB724200002000 UDI-DI Date3 Apr 2019ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
debritom+
Generic name
Surgical irrigation system nozzle
Model / reference
2000.0200
Primary DI / UDI-DI
B724200002000
FDA product code
FQH
GMDN term
Surgical irrigation system nozzle
Device class
Class II
Regulation number
880.5475
GUDID distribution status
Not in Commercial Distribution

Similar devices

Other devices filed under FDA product code FQH (Lavage, Jet).

Other devices from Medaxis AG

See all devices from Medaxis AG →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)