| Primary Device ID | 00613994610942 |
| NIH Device Record Key | 39971474-a04d-46af-b073-7927b47cbcab |
| Commercial Distribution Discontinuation | 2018-05-02 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Version Model Number | 1035D |
| 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 | false |
| Single Use | false |
| 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 |
| Length | 25 Feet |
| Length | 25 Feet |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00613994610942 [Primary] |
| LPB | Cardiac ablation percutaneous catheter |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2014-09-23 |
| 20199150023800 - NA | 2025-06-09 CUSTOM PACK BB11X70R1 5PK AV LOOP |
| 20199150023824 - NA | 2025-06-09 CUSTOM PACK BB8A44R4 4PK HBC MYO |
| 20199150024135 - NA | 2025-06-09 CUSTOM PACK BB11A07R2 5PK BRIDGE LINE |
| 00613994163523 - Duran AnCore | 2025-06-09 TOOL 7620HXL HANDLE DURAN ANCORE 14L |
| 00613994959546 - Open Pivot™ | 2025-06-09 ACCY 558 ACTUATOR PACKAGE AVG |
| 00643169402539 - MOSAIC ULTRA™ | 2025-06-09 SIZERS 7308U MOSAIC ULTRA AORTIC 26L |
| 00643169402591 - MOSAIC™CINCH™ | 2025-06-09 SIZERS 7308C MOSAIC CINCH AORTIC 26L |
| 00643169525511 - CG Future™ | 2025-06-09 SIZER SET 7638S CG FUTURE 26L |