| Primary Device ID | 00613994911599 | 
| NIH Device Record Key | 65abb532-5f73-4728-a226-8023b85e7ac7 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Version Model Number | 6W97R | 
| 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 | |
| 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 50 Degrees Celsius | 
| Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius | 
| Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius | 
| Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius | 
| Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius | 
| Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius | 
| Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius | 
| Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius | 
| Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius | 
| Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00613994911599 [Primary] | 
| DWE | TUBING, PUMP, CARDIOPULMONARY BYPASS | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 3 | 
| Public Version Date | 2018-07-06 | 
| Device Publish Date | 2016-05-22 | 
| 00763000763152 - NA | 2025-10-07 SW APP P7A2C11 ALTAVIVA CLINICIAN | 
| 00763000763817 - NA | 2025-10-07 SW APP P7A2P11 ALTAVIVA PATIENT | 
| 00763000929367 - Altaviva™ | 2025-10-07 KIT P7K2C001 ALTAVIVA CLINICIAN | 
| 00763000935627 - Altaviva™ | 2025-10-07 KIT P7K2P001 ALTAVIVA PATIENTA^ | 
| 00763000936433 - Altaviva™ | 2025-10-07 INS P7850N ALTAVIVA NEUROSTIMULATOR RC | 
| 00763000936440 - NA | 2025-10-07 ACCESSORY P71001 POCKET DISSECTOR | 
| 00199150050161 - NA | 2025-09-29 CUSTOM PACK HLO BB12D44R4 PUMP PK | 
| 00199150050178 - NA | 2025-09-29 CUSTOM PACK BB4W67R26 EVL ADULT E |