ampli-mini I 3 5P CIC-10 NWL PH 063-0532-0167

GUDID 07613389772838

Sonova AG

Air-conduction hearing aid, in-the-ear

• Primary Device ID: 07613389772838
• NIH Device Record Key: ed4bce76-8bc0-41d9-be50-fc7fe64cce38
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ampli-mini I 3 5P CIC-10 NWL PH
• Version Model Number: 10 NWL PH
• Catalog Number: 063-0532-0167
• Company DUNS: 480662550
• Company Name: Sonova AG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Conditional
• 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	07613389772838 [Primary]

FDA Product Code

• KLW: Masker, Tinnitus

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: 2024-11-20
• Device Publish Date: 2024-11-12

Devices Manufactured by Sonova AG

• 07613389772814 - ampli-mini I 5 5P CIC-10 NWL PH: 2024-11-20
• 07613389772821 - ampli-mini I 4 5P CIC-10 NWL PH: 2024-11-20
• 07613389772838 - ampli-mini I 3 5P CIC-10 NWL PH: 2024-11-20
• 07613389772838 - ampli-mini I 3 5P CIC-10 NWL PH: 2024-11-20
• 07613389772845 - ampli-mini I 2 5P CIC-10 NWL PH: 2024-11-20
• 07613389772852 - ampli-mini I 5 5P CIC-10 TI NWL PH: 2024-11-20
• 07613389772869 - ampli-mini I 4 5P CIC-10 TI NWL PH: 2024-11-20
• 07613389772913 - MEMINI I 5 5P CIC-10 NWL PH: 2024-11-20
• 07613389772920 - MEMINI I 4 5P CIC-10 NWL PH: 2024-11-20