Monarch RT 310
by Meridian Medical Systems, LLC
Monarch RT 310 is a Class II device made by Meridian Medical Systems, LLC, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00851354007135), 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 | Number00851354007135 | Date24 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00851354007135
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Monarch
- Generic name
- Flat panel x-ray detector integration unit
- Model / reference
- RT 310
- Primary DI / UDI-DI
- 00851354007135
- FDA product code
- MQB
- GMDN term
- Flat panel x-ray detector integration unit
- Device class
- Class II
- Regulation number
- 892.1680
- GUDID distribution status
- In Commercial Distribution
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