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Medline DEB001

by Medline Industries, Inc.

Medline DEB001 is a manual wound debridement tool (FDA Class I; FDA product code GED, Brush, Dermabrasion, Manual) made by Medline Industries, Inc., listed in FDA GUDID since 11 Jul 2024 (UDI-DI 10197344029686), 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 Number10197344029686 UDI-DI Date11 Jul 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  • Withdrawn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
Medline
Generic name
Manual wound debridement tool
Model / Ref / Catalog
DEB001
Primary DI / UDI-DI
10197344029686
FDA product code
GED
GMDN term
Manual wound debridement tool
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Wound debridement tool

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

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