| Primary Device ID | 00613994981387 |
| NIH Device Record Key | f07109b1-f9f6-4311-b5a2-6d2a19745c54 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 1035H |
| 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 | 40 Feet |
| Length | 40 Feet |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00613994981387 [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 | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2014-09-23 |
| 20763000651736 - Aortic Punch | 2025-03-31 Aortic Punch APU425 - 2.5mm punch size |
| 20763000651743 - Aortic Punch | 2025-03-31 Aortic Punch APU430 - 3.0mm punch size |
| 20763000651750 - Aortic Punch | 2025-03-31 Aortic Punch APU435 - 3.5mm punch size |
| 20763000651767 - Aortic Punch | 2025-03-31 Aortic Punch APU440 - 4.0mm punch size |
| 20763000651774 - Aortic Punch | 2025-03-31 Aortic Punch APU444 - 4.4mm punch size |
| 20763000651781 - Aortic Punch | 2025-03-31 Aortic Punch APU448 - 4.8mm punch size |
| 20763000651798 - Aortic Punch | 2025-03-31 Aortic Punch APU450 - 5.0mm punch size |
| 20763000651804 - Aortic Punch | 2025-03-31 Aortic Punch APU452 - 5.2mm punch size |