Co-Ease CE20LFNP
by Hemasource
Co-Ease CE20LFNP is a Class I device made by Hemasource, listed in FDA GUDID since 8 Dec 2022 (UDI-DI 00853614008272), 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 | Number00853614008272 | Date8 Dec 2022 | StatusListed |
Official records
- AccessGUDID record 00853614008272
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Co-Ease
- Generic name
- Non-adhesive device retention bandage
- Model / reference
- CE20LFNP
- Primary DI / UDI-DI
- 00853614008272
- FDA product code
- FQM
- GMDN term
- Non-adhesive device retention bandage
- Device class
- Class I
- Regulation number
- 880.5075
- GUDID distribution status
- In Commercial Distribution
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