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 |
Phone | 855-435-5477 |
csdepartment@ellipse-tech.com | |
Phone | 855-435-5477 |
csdepartment@ellipse-tech.com | |
Phone | 855-435-5477 |
csdepartment@nuvasive.com | |
Phone | 855-435-5477 |
csdepartment@nuvasive.com | |
Phone | 855-435-5477 |
csdepartment@nuvasive.com | |
Phone | 855-435-5477 |
csdepartment@nuvasive.com | |
Phone | 855-435-5477 |
csdepartment@nuvasive.com | |
Phone | 855-435-5477 |
csdepartment@nuvasive.com | |
Phone | 855-435-5477 |
csdepartment@nuvasive.com | |
Phone | 855-435-5477 |
csdepartment@nuvasive.com | |
Phone | 855-435-5477 |
csdepartment@nuvasive.com | |
Phone | 855-435-5477 |
csdepartment@nuvasive.com | |
Phone | 855-435-5477 |
csdepartment@nuvasive.com | |
Phone | 855-435-5477 |
csdepartment@nuvasive.com | |
Phone | 855-435-5477 |
csdepartment@nuvasive.com | |
Phone | 855-435-5477 |
csdepartment@nuvasive.com | |
Phone | 855-435-5477 |
csdepartment@nuvasive.com |
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 |