| Primary Device ID | 00858366007290 |
| NIH Device Record Key | e88697bc-9a23-4f31-879a-a99341d8deb7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SteriPath Gen2, 23G, 10ml |
| Version Model Number | 2710-23-EN |
| Catalog Number | 2710-23-EN |
| Company DUNS | 078603710 |
| Company Name | Magnolia Medical Technologies, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| 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 |
| 10858366007723 - Steripath Flow | 2025-12-03 Steripath Flow, 9in Luer, Wide Neck TA |
| 10858366007747 - Steripath Flow | 2025-12-03 Steripath Flow, 21G UltraTouch, Wide Neck TA |
| 10858366007761 - Steripath Flow | 2025-12-03 Steripath Flow, 23G UltraTouch, Wide Neck TA |
| 10858366007785 - Steripath Flow | 2025-12-03 Steripath Flow, 9in Luer, Long Neck TA |
| 10858366007808 - Steripath Flow | 2025-12-03 Steripath Flow, 21G UltraTouch, Long Neck TA |
| 10858366007822 - Steripath Flow | 2025-12-03 Steripath Flow, 23G UltraTouch, Long Neck TA |
| 10858366007846 - Steripath Flow | 2025-12-03 Steripath Flow, 7in Luer, 5mL Syringe |
| 10858366007860 - Steripath Flow | 2025-12-03 Steripath Flow, 23G UltraTouch, 5mL Syringe |