myAudioNova 4 088-0020-00042

GUDID 07613389793932

Sonova AG

Audiometric/hearing device software

• Primary Device ID: 07613389793932
• NIH Device Record Key: c2357927-7436-4513-ae05-b93bcfea5bb4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: myAudioNova 4
• Version Model Number: 4.2
• Catalog Number: 088-0020-00042
• Company DUNS: 480662550
• Company Name: Sonova AG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• 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	07613389793932 [Primary]

FDA Product Code

• OSM: Hearing Aid, Air-Conduction With Wireless Technology, Prescription

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-11-19
• Device Publish Date: 2024-11-11

On-Brand Devices [myAudioNova 4]

• 07613389793963: 4.3
• 07613389793932: 4.2
• 07613389793901: 4.1
• 07613389793871: 4.0