Neurosign 100 Pre-Amplifier

GUDID 05060229530356

THE MAGSTIM COMPANY LIMITED

Nerve-locating system, line-powered
Primary Device ID05060229530356
NIH Device Record Key15d9143b-53d5-4d27-a853-b641d0d12e63
Commercial Distribution StatusIn Commercial Distribution
Brand NameNeurosign 100 Pre-Amplifier
Version Model Number1719-00
Company DUNS500375274
Company NameTHE MAGSTIM COMPANY LIMITED
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+441994240798
EmailQA.RA@magstim.com

Device Identifiers

Device Issuing AgencyDevice ID
GS105060229530356 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

ETNStimulator, Nerve

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 Date2016-09-23

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