Aurix Newborn Hearing Screening System

GUDID 00062790880019

Main handheld unit for use with the Aurix system. The UDI is comprised of: GTIN + version/revision (VARIANT) + Date of Manufacture (PROD DATE) + Serial Number (SERIAL) The following devices are accessories for use with the Aurix system: 11002 Sound Stimulator DI: 00062790880026 11003 Amplifier DI: 00062790880033 11010 Laptop Computer DI: 00062790880040 100116 Amplifier Lead Cable DI:00062790880057 ER-3A-AUX Insert Earphones DI:00062790880064 100001 Electrodes DI: 00062790880071 100004 Ear Domes DI: 00062790880088 WA021 Tablet Computer DI:00062790880095

Vivosonic Inc

Evoked-potential audiometer
Primary Device ID00062790880019
NIH Device Record Keydecbcb6b-0530-4b07-8e54-1e31c472ae6f
Commercial Distribution StatusIn Commercial Distribution
Brand NameAurix Newborn Hearing Screening System
Version Model NumberAURIX-1
Company DUNS201740425
Company NameVivosonic 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 Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100062790880019 [Primary]

FDA Product Code

GWJStimulator, Auditory, Evoked Response

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-09-23

On-Brand Devices [Aurix Newborn Hearing Screening System ]

00062790880019Main handheld unit for use with the Aurix system. The UDI is comprised of: GTIN + version/rev
00627908080011Main handheld unit for use with the Aurix system. The UDI is comprised of: GTIN + version/rev

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