ampli-mini E 4 5P R-R AI PH 050-1060-P667

GUDID 07613389776973

Sonova AG

Air-conduction hearing aid, receiver-in-canal

• Primary Device ID: 07613389776973
• NIH Device Record Key: 59114ee1-64c9-4e76-a823-26e5d1512c79
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ampli-mini E 4 5P R-R AI PH
• Version Model Number: (silver gray)
• Catalog Number: 050-1060-P667
• 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	07613389776973 [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: 2025-08-26
• Device Publish Date: 2025-08-18

On-Brand Devices [ampli-mini E 4 5P R-R AI PH ]

• 07613389776980: (velvet black)
• 07613389776973: (silver gray)
• 07613389776966: (sandalwood)
• 07613389776959: (sand beige)