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Debrisoft Pad 10x10cm

by Lohmann & Rauscher International GmbH & Co KG

Debrisoft Pad 10x10cm (31222) is a manual wound debridement tool (FDA Class I; FDA product code NAB, Gauze / Sponge,Nonresorbable For External Use) made by Lohmann & Rauscher International GmbH & Co KG, listed in FDA GUDID since 17 Nov 2022 (UDI-DI 04021447537771), 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 Number04021447537771 UDI-DI Date17 Nov 2022ListedStatusListed 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  • Withdrawn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
Debrisoft
Generic name
Manual wound debridement tool
Model / Ref / Catalog
Pad 10x10cm, 31222
Primary DI / UDI-DI
04021447537771
FDA product code
NAB
GMDN term
Manual wound debridement tool
Device class
Class I
Regulation number
878.4014
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code NAB (Gauze / Sponge,Nonresorbable For External Use).

Other devices from Lohmann & Rauscher International GmbH & Co KG

See all devices from Lohmann & Rauscher International GmbH & Co KG →

Properties

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