Nexstim NBS System

GUDID 06430063200057

Nexstim NBS System

NEXSTIM, INC.

Stereotactic neuronavigation/planning system
Primary Device ID06430063200057
NIH Device Record Key81b2ba0e-7172-4ad6-96b7-d0318dc719b5
Commercial Distribution StatusIn Commercial Distribution
Brand NameNexstim NBS System
Version Model Number5
Company DUNS010845069
Company NameNEXSTIM, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+35892727170
Emailinfo@nexstim.com
Phone+35892727170
Emailinfo@nexstim.com
Phone+35892727170
Emailinfo@nexstim.com
Phone+35892727170
Emailinfo@nexstim.com
Phone+35892727170
Emailinfo@nexstim.com
Phone+35892727170
Emailinfo@nexstim.com
Phone+35892727170
Emailinfo@nexstim.com
Phone+35892727170
Emailinfo@nexstim.com
Phone+35892727170
Emailinfo@nexstim.com
Phone+35892727170
Emailinfo@nexstim.com
Phone+35892727170
Emailinfo@nexstim.com
Phone+35892727170
Emailinfo@nexstim.com

Device Identifiers

Device Issuing AgencyDevice ID
GS106430063200057 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GWFStimulator, Electrical, Evoked Response

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-21

On-Brand Devices [Nexstim NBS System]

06430063200057Nexstim NBS System
06430063200187Nexstim NBS System 6

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.