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debritom+ 1000.0501

by Medaxis AG

debritom+ 1000.0501 is a Class II device made by Medaxis AG, listed in FDA GUDID since 17 Apr 2026 (UDI-DI 07640407460811), 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 Number07640407460811 UDI-DI Date17 Apr 2026ListedStatusListed 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  • Withdrawn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
debritom+
Generic name
Surgical/orthopaedic lavage control unit
Model / reference
1000.0501
Primary DI / UDI-DI
07640407460811
FDA product code
FQH
GMDN term
Surgical/orthopaedic lavage control unit
Device class
Class II
Regulation number
880.5475
GUDID distribution status
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

  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)