| Primary Device ID | 00763000959838 |
| NIH Device Record Key | 92c722bb-2ade-4419-8eb5-72e8c3d1a815 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | BB11Q22R7 |
| Company DUNS | 006261481 |
| Company Name | MEDTRONIC, 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 | true |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com |
| Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00763000959838 [Primary] |
| 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 | 2024-07-05 |
| Device Publish Date | 2024-06-27 |
| 00763000879273 - Verify™ | 2024-07-05 ENS 353101 VERIFY ISTM US EMANUAL |
| 00763000879280 - Verify™ | 2024-07-05 ENS 353101 VERIFY ISTM US REFURB EMAN |
| 00763000959050 - NA | 2024-07-05 CUSTOM PACK BB11B31R7 CCS SUPP PK |
| 00763000959609 - NA | 2024-07-05 CUSTOM PACK BB10E56R15 COMBO |
| 00763000959760 - NA | 2024-07-05 CUSTOM PACK BB10L08R6 LYFLAT PK |
| 00763000959821 - NA | 2024-07-05 CUSTOM PACK BB11U53R1 E HEART L |
| 00763000959838 - NA | 2024-07-05CUSTOM PACK BB11Q22R7 LOURDES SUP P |
| 00763000959838 - NA | 2024-07-05 CUSTOM PACK BB11Q22R7 LOURDES SUP P |
| 00763000959845 - NA | 2024-07-05 CUSTOM PACK 12G61R1 NURSES |