Primary Device ID | 00887517164933 |
NIH Device Record Key | a18dab06-eeb9-417d-ab2c-7fab7a75670b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NVJJB |
Version Model Number | 2011302 |
Company DUNS | 053950783 |
Company Name | Nuvasive, 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(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887517164933 [Primary] |
IKN | Electromyograph, diagnostic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-26 |
00887517206152 | NVJJB Module II Electrodes, Wet Gel |
00887517206121 | NVJJB Needle Module II |
00887517205698 | NVJJB Module II |
00887517164933 | NV RM Network Cable, NVJJB IOM |
00887517164919 | NVJJB Retractor, Nerve |
00887517161307 | NVJJB Electrodes, Dual Wet Gel |
00887517061799 | NVJJB Insulator, InStim K-Wire Sterile |
00887517063489 | NVJJB Clips, Large Dynamic Stim Sterile |
00887517206169 | NVJJB MEP Add On Kit |
00887517084408 | NVJJB Module, Needle Electrode |
00887517062864 | NVJJB Clips, DST |
00887517054500 | NVJJB Probe |
00887517075376 | NVJJB EMG Harness Extensions |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NVJJB 85238486 4022531 Live/Registered |
Nuvasive, Inc. 2011-02-09 |