myPhonak Junior 2.0 088-0017-00020

GUDID 07613389637618

Sonova AG

Audiometric/hearing device software

• Primary Device ID: 07613389637618
• NIH Device Record Key: e0f70863-4ecc-45bf-a708-55706d9e9261
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: myPhonak Junior 2.0
• Version Model Number: 2.0
• Catalog Number: 088-0017-00020
• 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	07613389637618 [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: 2025-09-03
• Device Publish Date: 2025-08-26

Devices Manufactured by Sonova AG

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• 07613389637618 - myPhonak Junior 2.0: 2025-09-03
• 07613389637618 - myPhonak Junior 2.0: 2025-09-03
• 07613389836295 - DVD Phonak Target 11.1 DVD: 2025-09-02
• 07613389836301 - USB Phonak Target 11.1 USB: 2025-09-02
• 07613389836318 - Phonak Target 11.1: 2025-09-02
• 07613389776911 - ampli-mini E 5 5P R-R AI PH: 2025-08-26
• 07613389776928 - ampli-mini E 5 5P R-R AI PH: 2025-08-26
• 07613389776935 - ampli-mini E 5 5P R-R AI PH: 2025-08-26