| Primary Device ID | 00850030354327 |
| NIH Device Record Key | b39e066c-4c3e-4330-9378-783bdb0a32f6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | HydroPICC Dual Lumen |
| Version Model Number | 80H02102 |
| Catalog Number | 80H02102 |
| Company DUNS | 085539114 |
| Company Name | ACCESS VASCULAR, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850030354327 [Primary] |
| LJS | Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-12-27 |
| Device Publish Date | 2023-12-19 |
| 00850030354068 | HydroPICC Dual Lumen – Maximal Barrier Kit |
| 00850030354044 | HydroPICC 5Fr Dual Lumen Basic Kit (80cm GW) |
| 00850030354037 | HydroPICC 5Fr Dual Lumen Basic Kit (130cm GW) |
| 00850030354273 | HydroPICC Marked 5Fr Dual Lumen Maximal Barrier Kit |
| 00850030354266 | HydroPICC Marked 5Fr Dual Lumen Basic Kit (80cm GW) |
| 00850030354259 | HydroPICC Marked 5Fr Dual Lumen Basic Kit (130cm GW) |
| 00850030354334 | HydroPICC Marked 5Fr Dual Lumen Maximal Barrier Kit |
| 00850030354327 | HydroPICC Marked 5Fr Dual Lumen Basic Kit (70cm GW) |
| 00850030354310 | HydroPICC Marked 5Fr Dual Lumen Basic Kit (130cm GW) |
| 00850030354402 | 5F Dual Lumen Peripherally Inserted Central Marked Catheter (Mobile Kit) |