| Primary Device ID | 00643169771543 |
| NIH Device Record Key | 385b4a6d-455c-4a3c-b114-d62d04864db1 |
| Commercial Distribution Discontinuation | 2018-10-24 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Version Model Number | CB8B38R3 |
| 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 | true |
| 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 | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com |
| Storage Environment Temperature | Between 0 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 40 Degrees Celsius |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00643169771543 [Primary] |
| KFM | Pump, blood, cardiopulmonary bypass, non-roller type |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-01-04 |
| Device Publish Date | 2016-06-17 |
| 00763000643416 - OmniaSecure™ MRI SureScan™ | 2025-12-29 LEAD 3930M69 US MKT 69 CM DF4 MR EN |
| 00763000643430 - OmniaSecure™ MRI SureScan™ | 2025-12-29 LEAD 3930M74 US MKT 74 CM DF4 MR EN |
| 00763000643454 - OmniaSecure™ MRI SureScan™ | 2025-12-29 LEAD 3930M79 US MKT 79 CM DF4 MR EN |
| 00763000643478 - OmniaSecure™ MRI SureScan™ | 2025-12-29 LEAD 3930M84 US MKT 84 CM DF4 MR EN |
| 00763000643539 - OmniaSecure™ MRI SureScan™ | 2025-12-29 LEAD 3930M64 US MKT 64 CM DF4 MR EN |
| 00199150064052 - NA | 2025-12-23 CUSTOM PACK BB1B62R41 HLN CHR LNNT |
| 00199150064847 - NA | 2025-12-22 CUSTOM PACK BB12P57R3 HLO IOM FUS M |
| 00199150064861 - NA | 2025-12-22 CUSTOM PACK BB12S99R1 EVL NEONAT |