Primary Device ID | 00841983103650 |
NIH Device Record Key | 6d479da2-b23d-4725-bb43-27199ea827dd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NEUROFAX |
Version Model Number | NK-REVSUITE-MU |
Catalog Number | NK-REVSUITE-MU |
Company DUNS | 021063219 |
Company Name | NIHON KOHDEN AMERICA, 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 | false |
Lot Batch | false |
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)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841983103650 [Primary] |
OLT | Non-normalizing quantitative electroencephalograph software |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-24 |
00841983103988 | MEDICAL ISOLATION TRANSFORMER |
00841983103971 | NEUROFAX ACQUISITION, Dell Precision Tower desktop |
00841983103926 | EEG REVIEW SUITE, 5 USER LICENSE |
00841983103919 | EEG REVIEW SUITE, 10 USER LICENSE |
00841983103858 | LIVE VIEW PANEL SYSTEM |
00841983103841 | EEG REVIEW SYSTEM |
00841983103834 | 256 CHANNEL AMPLIFIER for JE-120A |
00841983103827 | 192 CHANNEL AMPLIFIER for JE-120A |
00841983103810 | 128 CHANNEL AMPLIFIER for JE-120A |
00841983103803 | NEUROFAX EEG DIGITAL, PORTABLE |
00841983103797 | NEUROFAX ACQUISITION, PANEL PC |
00841983103773 | NEUROFAX ACQUISITION, SML FRM |
00841983103650 | EEG REVIEW SUITE, MULTIUSE |
00841983103209 | NEUROFAX EEG DIGITAL, TOWER |
00841983102417 | Neurofax Electroencephalograph |
00841983104329 | NEUROFAX ACQUISITION, SML FRM |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NEUROFAX 73597401 1433703 Live/Registered |
NIHON KOHDEN CORPORATION 1986-05-07 |