Aurix Electrodes

GUDID 00062790880071

Electrodes for use with the Aurix system (DI: 00062790880019). The UDI is comprised of the following: GTIN (01) + EXPIRY (17) + BATCH/LOT (10)

Vivosonic Inc

Evoked-potential audiometer

• Primary Device ID: 00062790880071
• NIH Device Record Key: cd08eb42-cf6b-4aa1-b27f-9b1b1d5be3e9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Aurix Electrodes
• Version Model Number: 100001
• Company DUNS: 201740425
• Company Name: Vivosonic Inc
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00062790880071 [Primary]

FDA Product Code

• GWJ: Stimulator, Auditory, Evoked Response

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-23

On-Brand Devices [Aurix Electrodes ]

• 00062790880071: Electrodes for use with the Aurix system (DI: 00062790880019). The UDI is comprised of the fo
• 00627908080073: Electrodes for use with the Aurix system (DI: 00627908080011). The UDI is comprised of the fo