Compumedics Quik-Gel 92000015

GUDID 09342451003430

Electrolyte, Quik-Gel 16oz Jar

COMPUMEDICS LIMITED

Electrode conductive medium
Primary Device ID09342451003430
NIH Device Record Keya66a4b0f-d317-4f0d-827a-ddfda7a2aa02
Commercial Distribution StatusIn Commercial Distribution
Brand NameCompumedics Quik-Gel
Version Model NumberQuik-Gel Electrolyte
Catalog Number92000015
Company DUNS753750967
Company NameCOMPUMEDICS 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 Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+61384207386
Emailsupport@compumedics.com.au
Phone+61384207386
Emailsupport@compumedics.com.au
Phone+61384207386
Emailsupport@compumedics.com.au
Phone+61384207386
Emailsupport@compumedics.com.au
Phone+61384207386
Emailsupport@compumedics.com.au
Phone+61384207386
Emailsupport@compumedics.com.au
Phone+61384207386
Emailsupport@compumedics.com.au
Phone+61384207386
Emailsupport@compumedics.com.au
Phone+61384207386
Emailsupport@compumedics.com.au
Phone+61384207386
Emailsupport@compumedics.com.au

Device Identifiers

Device Issuing AgencyDevice ID
GS109342451003430 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GYBMedia, Electroconductive

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2026-03-20
Device Publish Date2026-03-12

On-Brand Devices [Compumedics Quik-Gel]

09342451003447Electrolyte Quick Gel 4oz Sample
09342451003430Electrolyte, Quik-Gel 16oz Jar
09342451003423Electrolyte, Quick-Gel 32oz Jar
09342451003416Electrolyte, Quick-Gel 128oz Jar

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