Corvus 14 210735
by Best Nomos
Corvus 14 210735 is a Class II device made by Best Nomos, listed in FDA GUDID since 29 Sep 2020 (UDI-DI 00852656007496), 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 | Number00852656007496 | Date29 Sep 2020 | StatusListed |
Official records
- AccessGUDID record 00852656007496
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Corvus 14
- Generic name
- Radiation therapy software
- Model / reference
- 210735
- Primary DI / UDI-DI
- 00852656007496
- FDA product code
- MUJ
- GMDN term
- Radiation therapy software
- Device class
- Class II
- Regulation number
- 892.5050
- GUDID distribution status
- In Commercial Distribution
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