| Primary Device ID | 00643169854956 |
| NIH Device Record Key | e0276543-3e89-4009-ae25-01acec3ab9f3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Sprinter Legend™ |
| Version Model Number | SPL12512WL |
| 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 | true |
| 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 | 12 Millimeter |
| Length | 12 Millimeter |
| Length | 12 Millimeter |
| Length | 12 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00643169854956 [Primary] |
| LOX | Catheters, transluminal coronary angioplasty, percutaneous |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-10-07 |
| Device Publish Date | 2018-01-14 |
| 00643169854970 | BLN SPL12520WL SPR LEGEND 1.25X20 OTW US |
| 00643169854963 | BLN SPL12515WL SPR LEGEND 1.25X15 OTW US |
| 00643169854956 | BLN SPL12512WL SPR LEGEND 1.25X12 OTW US |
| 00643169854949 | BLN SPL12510WL SPR LEGEND 1.25X10 OTW US |
| 00643169854932 | BLN SPL12506WL SPR LEGEND 1.25X6 OTW US |