| Primary Device ID | 00613994610935 |
| NIH Device Record Key | 1181e71a-a608-4464-9e04-3b6a5f9e1de4 |
| Commercial Distribution Discontinuation | 2018-05-02 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Version Model Number | 1035DW |
| 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 | 00613994610935 [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 |
| 00199150042098 - NA | 2025-09-08 CUSTOM PACK BB8B09R20 HLN OR INFANT |
| 00199150042661 - NA | 2025-09-08 CUSTOM PACK BB0C01R32 EVL 1/4 SUPPT |
| 00199150042753 - NA | 2025-09-08 CUSTOM PACK BB9F06R5 EVL WCH NEONA |
| 00199150043392 - NA | 2025-09-08 CUSTOM PACK BB12D74R5 HLO ALLIDON |
| 00199150043507 - NA | 2025-09-08 CUSTOM PACK BB12Q89R1 EVL 3/8 |
| 00199150043538 - NA | 2025-09-08 CUSTOM PACK BB12Q60R1 HLO ST BERNAR |
| 00199150044436 - NA | 2025-09-08 CUSTOM PACK BB9R01R23 HLN OR PEDIA |
| 20199150044454 - NA | 2025-09-08 CUSTOM PACK BB12R78R 5PK ACC PDEVL |