Kozee M21007
Kozee M21007 is a Class II device made by Sourcemark, LLC., listed in FDA GUDID since 27 Jan 2020 (UDI-DI 08973920006563), 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 | Number08973920006563 | Date27 Jan 2020 | StatusListed |
Official records
- AccessGUDID record 08973920006563
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Kozee
- Generic name
- Circulating-air whole-body heating system control unit
- Model / reference
- M21007
- Primary DI / UDI-DI
- 08973920006563
- FDA product code
- DWJ
- GMDN term
- Circulating-air whole-body heating system control unit
- Device class
- Class II
- Regulation number
- 870.5900
- GUDID distribution status
- In Commercial Distribution
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