| Primary Device ID | 20643169767533 |
| NIH Device Record Key | 6b458757-415f-4c49-9ba3-befee564916c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MVR™ |
| Version Model Number | CBMVR800 |
| 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 | false |
| 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 | false |
| OTC Over-The-Counter | false |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00643169767522 [Primary] |
| GS1 | 20643169767533 [Package] Contains: 00643169767522 Package: PK [6 Units] In Commercial Distribution |
| DTN | RESERVOIR, BLOOD, CARDIOPULMONARY BYPASS |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-01-22 |
| Device Publish Date | 2016-12-31 |
| 20643169767595 | RESERVOIR MVR800 VRB 800ML 6PK |
| 20643169767571 | RESERVOIR MVR1600 VRB 1600ML 6PK |
| 20643169767557 | RESERVOIR CBMVR1600 BIOACT STERILE 6PK |
| 20643169767533 | RESERVOIR CBMVR800 BIOACT STERILE 6PK |