Quasar 500-5005
Quasar 500-5005 is a Class I device made by Modus Medical Devices Inc, listed in FDA GUDID since 8 Dec 2022 (UDI-DI G34350050050), 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 | NumberG34350050050 | Date8 Dec 2022 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Quasar
- Generic name
- Multi-modality therapeutic radiation phantom, test object
- Model / reference
- 500-5005
- Primary DI / UDI-DI
- G34350050050
- FDA product code
- LHO
- GMDN term
- Multi-modality therapeutic radiation phantom, test object
- Device class
- Class I
- Regulation number
- 892.1940
- GUDID distribution status
- In Commercial Distribution
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