Primary Device ID | 00859945004143 |
NIH Device Record Key | 3934b4f1-ddb1-4f31-b528-3c707571e240 |
Commercial Distribution Discontinuation | 2018-09-08 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | V8 |
Version Model Number | TAV8-1722 |
Catalog Number | TAV8-1722 |
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 |