BE PLUS LTM PLUG-IN HEADBOX, 64CH (129-192)

GUDID 08056446900123

64 channels (129-192) patient-interface for EEG amplifier

EB NEURO SPA

Electroencephalograph
Primary Device ID08056446900123
NIH Device Record Keya1c33353-bde6-4ed4-95db-425f63b1ea1b
Commercial Distribution StatusIn Commercial Distribution
Brand NameBE PLUS LTM PLUG-IN HEADBOX, 64CH (129-192)
Version Model NumberB9630082040
Company DUNS339182263
Company NameEB NEURO SPA
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+390554565111
Emailinfo@ebneuro.com
Phone+390554565111
Emailinfo@ebneuro.com
Phone+390554565111
Emailinfo@ebneuro.com
Phone+390554565111
Emailinfo@ebneuro.com
Phone+390554565111
Emailinfo@ebneuro.com
Phone+390554565111
Emailinfo@ebneuro.com
Phone+390554565111
Emailinfo@ebneuro.com
Phone+390554565111
Emailinfo@ebneuro.com
Phone+390554565111
Emailinfo@ebneuro.com
Phone+390554565111
Emailinfo@ebneuro.com
Phone+390554565111
Emailinfo@ebneuro.com
Phone+390554565111
Emailinfo@ebneuro.com

Device Identifiers

Device Issuing AgencyDevice ID
GS108056446900123 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GWLAmplifier, Physiological Signal

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-06-03
Device Publish Date2019-05-24

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