| Primary Device ID | 00613994775832 |
| NIH Device Record Key | 0e3e3a7d-7c57-4310-8353-28f832cb0dc6 |
| Commercial Distribution Discontinuation | 2018-05-02 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Version Model Number | 1035E |
| 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 | 30 Feet |
| Length | 30 Feet |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00613994775832 [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 |
| 00199150031610 - NA | 2025-07-21 CUSTOM PACK BB1U06R24 CHRIS AD |
| 00199150032464 - NA | 2025-07-21 CUSTOM PACK BB10R35R4 CP PRIME |
| 20199150032482 - NA | 2025-07-21 CUSTOM PACK 6S19R4 10PK DIALYSIS |
| 00199150033423 - NA | 2025-07-21 CUSTOM PACK BB12B90R7 SPECTRU |
| 20199150033571 - NA | 2025-07-21 CUSTOM PACK BB2U59R3 2PK 1/4 TBL L |
| 00199150033614 - NA | 2025-07-21 CUSTOM PACK BB10J74R14 3/8CNTRIS |
| 00199150034246 - NA | 2025-07-21 CUSTOM PACK BB11J86R12 ADULT E |
| 00763000925093 - FlexCath Cross™ Transseptal Solution | 2025-07-21 NDL 900302 FLEXCATH CROSS SL 63CM EIFU |