CorPath GRX Robotic Drive 303
CorPath GRX Robotic Drive 303 is a Class II device made by Corindus, Inc., listed in FDA GUDID since 20 Jan 2017 (UDI-DI 00816280023031), not in commercial distribution (GUDID) 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 | Number00816280023031 | Date20 Jan 2017 | StatusListed |
Official records
- AccessGUDID record 00816280023031
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- CorPath GRX Robotic Drive
- Generic name
- Cardiac mapping system workstation
- Model / Ref / Catalog
- 303
- Primary DI / UDI-DI
- 00816280023031
- FDA product code
- DXX
- GMDN term
- Cardiac mapping system workstation
- Device class
- Class II
- Regulation number
- 870.1290
- GUDID distribution status
- Not in Commercial Distribution
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