| Primary Device ID | 00816280023116 |
| NIH Device Record Key | b6159bb2-2d15-40fa-b029-9a7c9edeec84 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CorPath GRX Drape, Control Console |
| Version Model Number | 311 |
| Catalog Number | 311 |
| Company DUNS | 781746586 |
| Company Name | CORINDUS, INC. |
| Device Count | 4 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00816280023109 [Unit of Use] |
| GS1 | 00816280023116 [Primary] |
| DXX | System, Catheter Control, Steerable |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2017-01-20 |
| 00816280023185 - CorPath GRX Cassette Duo | 2022-08-16 |
| 00816280022010 - CorPath 200 Control Console | 2019-09-11 |
| 00816280022027 - CorPath 200 Articulated Arm | 2019-09-11 |
| 00816280022034 - CorPath 200 Robotic Drive | 2019-09-11 |
| 00816280022041 - CorPath 200 Cassette | 2019-09-11 |
| 00816280022072 - CorPath 200 POGO Pin Caps | 2019-09-11 |
| 00816280022096 - CorPath 200 Control Console Drape | 2019-09-11 |
| 00816280022119 - CorPath 200 Joystick Covers | 2019-09-11 |