Phonak Audéo ISphereTrial 050-1030-9ABA

GUDID 07613389808117

Sonova AG

Air-conduction hearing aid, receiver-in-canal

• Primary Device ID: 07613389808117
• NIH Device Record Key: d6b0ecc1-5c7f-4630-afea-5de48182a8a1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Phonak Audéo ISphereTrial
• Version Model Number: (atlantic green)
• Catalog Number: 050-1030-9ABA
• 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	07613389808117 [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: 2025-01-16
• Device Publish Date: 2025-01-08

On-Brand Devices [Phonak Audéo ISphereTrial ]

• 07613389699180: (atlantic green)
• 07613389583038: (silver gray)
• 07613389808148: (silver gray)
• 07613389808131: (silver gray)
• 07613389808124: (atlantic green)
• 07613389808117: (atlantic green)