| Primary Device ID | 10803622106481 |
| NIH Device Record Key | f1021c9e-327f-420c-b94f-fba5e0386662 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Ventricular vent catheter |
| Version Model Number | VT-xxxxx |
| Company DUNS | 080914995 |
| Company Name | LIVANOVA USA, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00803622106484 [Primary] |
| GS1 | 10803622106481 [Package] Contains: 00803622106484 Package: CASE [10 Units] In Commercial Distribution |
| DWF | CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-08-15 |
| Device Publish Date | 2015-07-16 |
| 10803622106498 | VT-xxxxx |
| 10803622106481 | VT-xxxxx |
| 10803622106474 | VT-xxxxx |
| 10803622106467 | VT-xxxxx |
| 10803622106450 | VT-xxxxx |
| 10803622106443 | VT-xxxxx |
| 10803622106436 | VT-xxxxx |
| 10803622106429 | VT-xxxxx |
| 10803622106412 | VT-xxxxx |
| 10803622106405 | VT-xxxxx |
| 10803622106399 | VT-xxxxx |
| 10803622106382 | VT-xxxxx |
| 10803622106375 | VT-xxxxx |
| 10803622106368 | VT-xxxxx |
| 10803622106351 | VT-xxxxx |
| 10803622106344 | VT-xxxxx |
| 10803622106337 | VT-xxxxx |
| 10803622106320 | VT-xxxxx |