Debrisoft Lolly
by Lohmann & Rauscher International GmbH & Co KG
Debrisoft Lolly (33224) is a manual wound debridement tool (FDA Class I; FDA product code GDY, Gauze/Sponge, Internal, X-Ray Detectable) made by Lohmann & Rauscher International GmbH & Co KG, listed in FDA GUDID since 7 Jun 2023 (UDI-DI 04056649025665), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04056649025665 | Date7 Jun 2023 | StatusListed |
Official records
- AccessGUDID record 04056649025665
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Debrisoft
- Generic name
- Manual wound debridement tool
- Model / Ref / Catalog
- Lolly, 33224
- Primary DI / UDI-DI
- 04056649025665
- FDA product code
- GDY
- GMDN term
- Manual wound debridement tool
- Device class
- Class I
- Regulation number
- 878.4450
- GUDID distribution status
- In Commercial Distribution
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