| Primary Device ID | 00899054002203 |
| NIH Device Record Key | 86e084cb-50a6-4542-9fe6-56716ab3bfdf |
| Commercial Distribution Discontinuation | 2020-02-06 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Triumph Aortic Perfusion Cannula |
| Version Model Number | MPH-0022S |
| Company DUNS | 791048924 |
| Company Name | KDL MEDICAL, INC. |
| Device Count | 1 |
| 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 | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |