| Primary Device ID | 00812258026899 |
| NIH Device Record Key | 81907428-d4ca-4508-8c68-78f4d6148b86 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MAGEC® Wand |
| Version Model Number | MML-001 |
| Catalog Number | MML-001 |
| Company DUNS | 837845234 |
| Company Name | NUVASIVE SPECIALIZED ORTHOPEDICS, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00812258026899 [Primary] |
| LXH | Orthopedic Manual Surgical Instrument |
| PGN | Growing Rod System- Magnetic Actuation |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-04-25 |
| Device Publish Date | 2015-12-23 |
| 00812258026899 | Magnet locator - for use with the MAGEC® Spinal Bracing and Distraction System |
| 00812258022259 | Magnet locator - for use with the MAGEC® Spinal Bracing and Distraction System |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MAGEC 86711404 not registered Dead/Abandoned |
NUVASIVE, INC. 2015-07-31 |
![]() MAGEC 77886556 4411323 Live/Registered |
NUVASIVE, INC. 2009-12-04 |
![]() MAGEC 73408690 1270642 Dead/Cancelled |
Al Lee & Associates, Inc. 1983-01-10 |