Phonak Audéo E-Sphere 050-1213-P6

GUDID 07613389870473

Sonova AG

Air-conduction hearing aid, receiver-in-canal

• Primary Device ID: 07613389870473
• NIH Device Record Key: 967d33df-0197-47f8-92bf-4750f93452f7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Phonak Audéo E-Sphere
• Version Model Number: Demo
• Catalog Number: 050-1213-P6
• 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: false
• Serial Number: true
• 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	07613389870473 [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: 2026-03-25
• Device Publish Date: 2026-03-17

Devices Manufactured by Sonova AG

• 07613389755763 - Phonak Audéo E50-R: 2026-03-25
• 07613389755770 - Phonak Audéo E30-R: 2026-03-25
• 07613389759112 - Phonak Audéo E90-Sphere: 2026-03-25
• 07613389759129 - Phonak Audéo E70-Sphere: 2026-03-25
• 07613389759136 - Phonak Audéo E50-Sphere: 2026-03-25
• 07613389759150 - Phonak Audéo E-R Trial: 2026-03-25
• 07613389759174 - Phonak Audéo ESphereTrial: 2026-03-25
• 07613389761917 - Phonak Audéo E30-R: 2026-03-25