| Primary Device ID | 00859945004099 |
| NIH Device Record Key | b40175e1-a214-41bc-82a8-237e6526d197 |
| Commercial Distribution Discontinuation | 2018-09-08 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | V8 |
| Version Model Number | 232812C110 |
| Catalog Number | 232812C110 |
| Company DUNS | 037375827 |
| Company Name | INTERVALVE 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 | 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 |
| 00859945004174 | V8 Balloon Aortic Valvuloplasty Catheter, TAV8-2328 |
| 00859945004167 | V8 Balloon Aortic Valvuloplasty Catheter, TAV8-2126 |
| 00859945004150 | V8 Balloon Aortic Valvuloplasty Catheter, TAV8-1924 |
| 00859945004143 | V8 Balloon Aortic Valvuloplasty Catheter, TAV8-1722 |
| 00859945004136 | V8 Balloon Aortic Valvuloplasty Catheter, V8-2328 |
| 00859945004129 | V8 Balloon Aortic Valvuloplasty Catheter, V8-2126 |
| 00859945004112 | V8 Balloon Aortic Valvuloplasty Catheter, V8-1924 |
| 00859945004105 | V8 Balloon Aortic Valvuloplasty Catheter, V8-1722 |
| 00859945004099 | V8 Balloon Aortic Valvuloplasty Catheter, 232812C110 |
| 00859945004082 | V8 Balloon Aortic Valvuloplasty Catheter, 212612C110 |
| 00859945004075 | V8 Balloon Aortic Valvuloplasty Catheter, 192412C110 |
| 00859945004068 | V8 Balloon Aortic Valvuloplasty Catheter, 172212C110 |