Dermacea 441507
Dermacea 441507 is a Class I device made by Cardinalhealth, listed in FDA GUDID since 27 Jun 2018 (UDI-DI 10884527021055), 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 | Number10884527021055 | Date27 Jun 2018 | StatusListed |
Official records
- AccessGUDID record 10884527021055
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Dermacea
- Generic name
- Pressure bandage, non-latex, sterile
- Model / Ref / Catalog
- 441507
- Primary DI / UDI-DI
- 10884527021055
- FDA product code
- FQM
- GMDN term
- Pressure bandage, non-latex, sterile
- Device class
- Class I
- Regulation number
- 880.5075
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 12 FeetWidth — 6 Inch
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