| Primary Device ID | 00816280021051 |
| NIH Device Record Key | 154e7e68-68e5-49e0-ab05-37608bd6464d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CorPath Imaging System |
| Version Model Number | 105 |
| Catalog Number | 105 |
| Company DUNS | 781746586 |
| Company Name | CORINDUS, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00816280021051 [Primary] |
| OUG | Medical Device Data System |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2017-01-25 |
| 00816280021068 | 106 |
| 00816280021051 | 105 |