| Primary Device ID | 00681490023429 |
| NIH Device Record Key | 6001ee19-f01c-4fad-9d9c-8b19cb01626d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Lesinski |
| Version Model Number | 0436 |
| Company DUNS | 835465063 |
| Company Name | MEDTRONIC XOMED, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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 | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com |
| Length | 4.75 Millimeter |
| Length | 4.75 Millimeter |
| Length | 4.75 Millimeter |
| Length | 4.75 Millimeter |
| Length | 4.75 Millimeter |
| Length | 4.75 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 4.75 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 4.75 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 4.75 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 4.75 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 4.75 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 4.75 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 4.75 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 4.75 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 4.75 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 4.75 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 4.75 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00681490023429 [Primary] |
| LTB | CYCLOSPORINE RADIOIMMUNOASSAY |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-04-29 |
| 00681490024259 | PROSTHESIS 0532 LESINSKI FLEX H/A TOTAL |
| 00681490024235 | PROSTHESIS 0531 LESINSKI FLEX H/A PART |
| 00681490024198 | PROSTHESIS 0530 LESINSKI FLEX H/A TOTAL |
| 00681490023436 | PROSTHESIS 0437 LESINSKI MOD LOOP 4.25MM |
| 00681490023429 | PROSTHESIS 0436 LESINSKI FLPL/PLATINUM |
| 00681490023412 | PROSTHESIS 0435 LESINSKI MOD LOOP 4.5MM |
| 00681490023337 | PROSTHESIS 0429 PISTON .6X4.75 PLAT/FLPL |
| 00681490023320 | PROSTHESIS 0428 PISTON .6X4.5 PLAT/FLPL |
| 00681490023313 | PROSTHESIS 0427 PISTON .6X4.25 PLT/FLPL |
| 00681490017664 | PROSTHESIS 0320 STAPEDOTOMY REVISION |
| 00763000034320 | PROSTHESIS 0429 PISTON .6X4.75 PLAT/FLPL |
| 00763000034313 | PROSTHESIS 0428 PISTON .6X4.5 PLAT/FLPL |
| 00763000033286 | PROSTHESIS 0427 PISTON .6X4.25 PLT/FLPL |