| Primary Device ID | 38033178019126 |
| NIH Device Record Key | 7a70e31f-c1cd-4afc-8584-5d3a6ea31d5f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Ventricular Vent Catheter |
| Version Model Number | VT-84413 |
| Company DUNS | 442126587 |
| Company Name | SORIN GROUP ITALIA SRL |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08033178019125 [Primary] |
| GS1 | 38033178019126 [Package] Contains: 08033178019125 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 | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2026-02-19 |
| Device Publish Date | 2026-02-11 |
| 38033178019218 | VT-92116 |
| 38033178019201 | VT-89620 |
| 38033178019188 | VT-89616 |
| 38033178019171 | VT-89420 |
| 38033178019164 | VT-89418 |
| 38033178019157 | VT-89416 |
| 38033178019126 | VT-84413 |
| 38033178019119 | VT-84410 |
| 38033178019102 | VT-83116 |
| 38033178019096 | VT-63218 |
| 38033178019089 | VT-57320 |
| 38033178019072 | VT-57316 |
| 38033178019065 | VT-53218 |
| 38033178019058 | VT-46118 |
| 38033178019041 | VT-31212 |