myPhonak 7 088-0022-00072

GUDID 07613389779271

Sonova AG

Audiometric/hearing device software

• Primary Device ID: 07613389779271
• NIH Device Record Key: 74c259fc-4b0c-4322-9536-cbaa4ed85c18
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: myPhonak 7
• Version Model Number: 7.2
• Catalog Number: 088-0022-00072
• 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	07613389779271 [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 [myPhonak 7]

• 07613389759259: 7.0
• 07613389779271: 7.2
• 07613389779257: 7.1