Primary Device ID | 06430063200187 |
NIH Device Record Key | 4c9d45ff-8e53-4389-8632-97c3c8253acf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Nexstim NBS System |
Version Model Number | 6 |
Company DUNS | 010845069 |
Company Name | NEXSTIM, 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 | 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 |
Phone | +35892727170 |
info@nexstim.com | |
Phone | +35892727170 |
info@nexstim.com | |
Phone | +35892727170 |
info@nexstim.com | |
Phone | +35892727170 |
info@nexstim.com | |
Phone | +35892727170 |
info@nexstim.com | |
Phone | +35892727170 |
info@nexstim.com | |
Phone | +35892727170 |
info@nexstim.com | |
Phone | +35892727170 |
info@nexstim.com | |
Phone | +35892727170 |
info@nexstim.com | |
Phone | +35892727170 |
info@nexstim.com | |
Phone | +35892727170 |
info@nexstim.com | |
Phone | +35892727170 |
info@nexstim.com | |
Phone | +35892727170 |
info@nexstim.com | |
Phone | +35892727170 |
info@nexstim.com | |
Phone | +35892727170 |
info@nexstim.com | |
Phone | +35892727170 |
info@nexstim.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06430063200187 [Primary] |
GWF | Stimulator, Electrical, Evoked Response |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-04-09 |
Device Publish Date | 2025-04-01 |
06430063200057 | Nexstim NBS System |
06430063200187 | Nexstim NBS System 6 |