Sirona RX22673
by Datrix LLC
Sirona RX22673 is a Class II device made by Datrix LLC, listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00851074007125), 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 | Number00851074007125 | Date23 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00851074007125
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Sirona
- Generic name
- Telemetric electrocardiographic ambulatory recorder
- Model / reference
- RX22673
- Primary DI / UDI-DI
- 00851074007125
- FDA product code
- MWJ
- GMDN term
- Telemetric electrocardiographic ambulatory recorder
- Device class
- Class II
- Regulation number
- 870.2800
- GUDID distribution status
- In Commercial Distribution
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