FlannelPlus™ 77983
FlannelPlus™ 77983 (DUP77983) is a Class I device made by Derma Sciences Canada, Inc, listed in FDA GUDID since 13 Nov 2018 (UDI-DI 00809958077719), registry data as of 22 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 | Number00809958077719 | Date13 Nov 2018 | StatusListed |
Official records
- AccessGUDID record 00809958077719
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- FlannelPlus™
- Generic name
- Woven gauze roll/sheet
- Model / Ref / Catalog
- 77983, DUP77983
- Primary DI / UDI-DI
- 00809958077719
- FDA product code
- FQM
- GMDN term
- Woven gauze roll/sheet
- Device class
- Class I
- Regulation number
- 880.5075
- GUDID distribution status
- In Commercial Distribution
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Other devices from DERMA SCIENCES CANADA, INC (dba DERMA SCIENCES, INC.)
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