Hydrofera Blue HBRT8080
Hydrofera Blue HBRT8080 is a device classified as Unclassified made by Hydrofera, LLC, listed in FDA GUDID since 1 Jun 2018 (UDI-DI 20854827008053), 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 | Number20854827008053 | Date1 Jun 2018 | StatusListed |
Official records
- AccessGUDID record 20854827008053
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Hydrofera Blue
- Generic name
- Wound-nonadherent dressing, permeable, antimicrobial
- Model / reference
- HBRT8080
- Primary DI / UDI-DI
- 20854827008053
- FDA product code
- FRO
- GMDN term
- Wound-nonadherent dressing, permeable, antimicrobial
- Device class
- U
- GUDID distribution status
- In Commercial Distribution
- Size
- Width — 8 InchHeight — 8 Inch
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