Phonak Naída L30-M 050-1164-H0

GUDID 07613389841831

Sonova AG

Air-conduction hearing aid, behind-the-ear

• Primary Device ID: 07613389841831
• NIH Device Record Key: 8164e593-d8a6-4bbe-9ca1-810b5ab1008e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Phonak Naída L30-M
• Version Model Number: (beige)
• Catalog Number: 050-1164-H0
• 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	07613389841831 [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: 2025-09-04
• Device Publish Date: 2025-08-27

Devices Manufactured by Sonova AG

• 07613389841831 - Phonak Naída L30-M: 2025-09-04
• 07613389841831 - Phonak Naída L30-M: 2025-09-04
• 07613389637618 - myPhonak Junior 2.0: 2025-09-03
• 07613389836295 - DVD Phonak Target 11.1 DVD: 2025-09-02
• 07613389836301 - USB Phonak Target 11.1 USB: 2025-09-02
• 07613389836318 - Phonak Target 11.1: 2025-09-02
• 07613389776911 - ampli-mini E 5 5P R-R AI PH: 2025-08-26
• 07613389776928 - ampli-mini E 5 5P R-R AI PH: 2025-08-26
• 07613389776935 - ampli-mini E 5 5P R-R AI PH: 2025-08-26