DeRoyal 15-019
DeRoyal 15-019 is a Class I device made by Deroyal Industries, Inc., listed in FDA GUDID since 2 Feb 2023 (UDI-DI 00749756334280), 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 | Number00749756334280 | Date2 Feb 2023 | StatusListed |
Official records
- AccessGUDID record 00749756334280
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- DeRoyal
- Generic name
- Wound-nonadherent dressing, permeable, non-antimicrobial
- Model / Ref / Catalog
- 15-019
- Primary DI / UDI-DI
- 00749756334280
- FDA product code
- NAB
- GMDN term
- Wound-nonadherent dressing, permeable, non-antimicrobial
- Device class
- Class I
- Regulation number
- 878.4014
- GUDID distribution status
- In Commercial Distribution
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