| Primary Device ID | 10850984007086 |
| NIH Device Record Key | 7afacdd4-5c6c-4148-9165-5bdb4f82b5de |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PIVO 24G |
| Version Model Number | 202-0011 |
| Catalog Number | 202-0011 |
| Company DUNS | 079714011 |
| Company Name | VELANO VASCULAR, 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 |
| Needle Gauge | 24 Gauge |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850984007089 [Primary] |
| GS1 | 10850984007086 [Package] Contains: 00850984007089 Package: Carton [50 Units] In Commercial Distribution |
| JKA | Tubes, Vials, Systems, Serum Separators, Blood Collection |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-12-24 |
| Device Publish Date | 2019-12-16 |
| 10850984007086 - PIVO 24G | 2019-12-2424G Compatible PIVO Blood draw device |
| 10850984007086 - PIVO 24G | 2019-12-24 24G Compatible PIVO Blood draw device |
| 00850984007027 - PIVO 20G | 2019-04-23 PIVO (2.0) 20G compatible device. |
| 00850984007034 - PIVO 22G | 2019-04-23 PIVO (2.0) 22G Compatible device |
| 10850984007000 - PIVO 20G | 2018-07-12 PIVO 20G compatible device. Formerly TIVA. |
| 10850984007017 - PIVO 22G | 2018-07-12 PIVO 22G Compatible device |