ampli-charge I 1 5P 075-0075-12067

GUDID 07613389629316

Sonova AG

Noninvasive device battery charger

• Primary Device ID: 07613389629316
• NIH Device Record Key: af3ef95e-3a6c-40b2-83ab-a2203b65e95d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ampli-charge I 1 5P
• Version Model Number: EU EPS
• Catalog Number: 075-0075-12067
• 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	07613389629316 [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 [ampli-charge I 1 5P ]

• 07613389793024: US EPS
• 07613389793017: no EPS
• 07613389629316: EU EPS