Primary Device ID | 04931921007631 |
NIH Device Record Key | 29e00ed0-8c9f-4ade-b0cd-1729b2a24052 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Nihon Kohden, EEG-1200A Series Neurofax |
Version Model Number | JE-921A-01 |
Catalog Number | JE-921A-01 |
Company DUNS | 690568050 |
Company Name | NIHON KOHDEN CORPORATION |
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 | false |
Serial Number | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04931921007631 [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 | 2022-11-28 |
Device Publish Date | 2019-07-24 |
04931921007716 | Flash lamp assembly, Round shape |
04931921007709 | Flash lamp assembly |
04931921007631 | Electrode junction box, Standard accessory |
04931921007730 | Cart, Compact type, used with EEG-1200A, works with standard and optional accessories |
04931921007723 | Cart, used with EEG-1200A, works with standard and optional accessories |