| Primary Device ID | 20643169596584 |
| NIH Device Record Key | 08212cc3-3b9c-4ee1-b1fe-590eb1ae20d4 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | DLP8M07R2 |
| Company DUNS | 006261481 |
| Company Name | MEDTRONIC, INC. |
| Device Count | 5 |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00643169596573 [Unit of Use] |
| GS1 | 20643169596584 [Primary] |
| DWF | CATHETER, CANNULA AND TUBING, VASCULAR, 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 | 2016-06-05 |
| 20199150061970 - NA | 2025-12-08 CUSTOM PACK BB12R02R3 5PK ACC STRNG SUC |
| 00199150062027 - NA | 2025-12-08 CUSTOM PACK BB12R85R AVL 3/8 ECCPK |
| 20199150062229 - NA | 2025-12-08 CUSTOM PACK BB1Q47R3 5PK ACC TABLE |
| 20199150062243 - NA | 2025-12-08 CUSTOM PACK BB12R66R 20PK ACC 1/4 W/LL |
| 20199150062960 - NA | 2025-12-08 CUSTOM PACK BB9R13R15 4PK CPN PLEG PACK |
| 00643169265691 - NA | 2025-12-08 LEAD ACC KIT 6056M GLOBAL 17L NEW ACI |
| 00199150060467 - NA | 2025-11-28 CUSTOM PACK BB11Q49R14 EVL 3/8 EC |
| 00199150060627 - NA | 2025-11-28 CUSTOM PACK BB12M28R9 HLO QHLM-FROS |