| Primary Device ID | 00894912002142 |
| NIH Device Record Key | d54ebe23-9737-4f7c-b609-dc9f7ef1b52d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CT |
| Version Model Number | CT-XT |
| Catalog Number | CT-XT |
| Company DUNS | 069261402 |
| Company Name | KOVEN TECHNOLOGY, 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 |