DermaForm 502092
DermaForm 502092 is a device classified as Unclassified made by Geistlich Pharma AG, listed in FDA GUDID since 19 Oct 2026 (UDI-DI 07610221017621), registry data as of 2 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number07610221017621 | Date19 Oct 2026 | StatusListed |
Official records
- AccessGUDID record 07610221017621
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- DermaForm
- Generic name
- Animal-derived wound matrix dressing
- Model / reference
- 502092
- Primary DI / UDI-DI
- 07610221017621
- FDA product code
- KGN
- GMDN term
- Animal-derived wound matrix dressing
- Device class
- U
- GUDID distribution status
- In Commercial Distribution
- Size
- Weight — 500 Milligram
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