Primary Device ID | 00841983104268 |
NIH Device Record Key | bdc28ff1-2cbe-4dd6-8da8-5fd94ce281ad |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Neuropack S3 |
Version Model Number | NPS3-LT-Cart4-ZA |
Catalog Number | MEB-9600 |
Company DUNS | 021063219 |
Company Name | NIHON KOHDEN AMERICA, 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 | false |
Serial Number | true |
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 Issuing Agency | Device ID |
---|---|
GS1 | 00841983104268 [Primary] |
IKN | Electromyograph, diagnostic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-07-28 |
Device Publish Date | 2020-07-20 |
00841983104268 | Preassembled MEB-9600 on Cart for MEB-9600 Neuropack S3 desktop system, performs Evoked potentia |
00841983104251 | Preassembled MEB-9600 on Cart for MEB-9600 Neuropack S3 desktop system, performs Evoked potentia |