Amplifon Brand

GUDID 07613389502183

ampli-charge R 2 (no EPS)

Sonova AG

Noninvasive device battery charger

• Primary Device ID: 07613389502183
• NIH Device Record Key: 083570a2-fe92-41cf-8a95-466e72cba9d3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Amplifon Brand
• Version Model Number: 075-0048-10067
• 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	07613389502183 [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: 2023-05-03
• Device Publish Date: 2023-04-25

On-Brand Devices [Amplifon Brand]

• 07613389399608: ampli-energy R trial P (silver gray)
• 07613389399554: ampli-connect R trial P (silver gray)
• 07613389434743: ampli-energy B trial P (silver gray)
• 07613389434736: ampli-energy B 2 P RP PH (silver gray)
• 07613389434729: ampli-energy B 2 P RP PH (sand beige)
• 07613389434712: ampli-energy B 3 P RP PH (silver gray)
• 07613389434309: ampli-energy B 3 P RP PH (sand beige)
• 07613389434293: ampli-energy B 4 P RP PH (silver gray)
• 07613389434286: ampli-energy B 4 P RP PH (sand beige)
• 07613389434279: ampli-energy B 5 P RP PH (silver gray)
• 07613389434262: ampli-energy B 5 P RP PH (sand beige)
• 07613389502190: ampli-charge R 2 (EU EPS)
• 07613389502183: ampli-charge R 2 (no EPS)