| 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 |
| 00763000574598 - NA | 2025-02-18 COMMUNICATOR TM90T0 PROX US EMANUAL |
| 00763000579388 - N/A | 2025-02-18 TELEMETRY MODULE TM90Q0 ISTIM X US |
| 00763000879297 - NA | 2025-02-18 TELEMETRY TM90Q0 ISTIM X US EMAN |
| 00763000988777 - NA | 2025-02-17 CUSTOM PACK BB6Z71R15 VA |
| 20763000998145 - NA | 2025-02-17 CUSTOM PACK SSBB12N37R 10PK LOWER LMB |
| 00763000998424 - NA | 2025-02-17 CUSTOM PACK BB10Z65R1 V A D |
| 00763000517830 - Hancock™ | 2025-02-14 CONDUIT HC15022 HK1 MO 26L |
| 00763000995775 - NA | 2025-02-14 CUSTOM PACK BB11W65R2 SPECTRUM CPB |