| Primary Device ID | 00613994775856 |
| NIH Device Record Key | 8d59cf32-ffb7-42a4-a89c-6f2e0b679bb1 |
| Commercial Distribution Discontinuation | 2018-05-02 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Version Model Number | 1035F |
| 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 | 00613994775856 [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 |
| 00199150033478 - NA | 2026-03-10 RECHARGE SYSTEM RS7230 US INCEPTIV |
| 20199150071313 - NA | 2026-03-10 CUSTOM PACK BB12Q91R 5PK ACC 1/4 INC |
| 20199150071337 - NA | 2026-03-10 CUSTOM PACK BB12T57R 5PK ACC BARNES DPC |
| 20199150071641 - NA | 2026-03-10 CUSTOM PACK BB12T16R1 2PK AVL ENDEAVOR |
| 20199150071665 - NA | 2026-03-10 CUSTOM PACK BB12S13R1 5PK AVL 3/8 |
| 00199150071678 - NA | 2026-03-10 CUSTOM PACK BB5G80R37 E. 1/4 PK |
| 20199150071832 - NA | 2026-03-10 CUSTOM PACK BB12T25R 5PK ACC COATED COM |
| 00199150071845 - NA | 2026-03-10 CUSTOM PACK BB12B01R5 EVL PEDS C |