Neosonic

GUDID 06945936703448

Xiamen New Sound Technology Co., Ltd.

Air-conduction hearing aid, in-the-ear

• Primary Device ID: 06945936703448
• NIH Device Record Key: 8853c3d7-e092-4985-9495-fe9b1583daf3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Neosonic
• Version Model Number: Neosonic BT-Omni
• Company DUNS: 528181200
• Company Name: Xiamen New Sound Technology Co., Ltd.
• Device Count: 2
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• 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	06945936703448 [Unit of Use]
GS1	16945936703445 [Primary]

FDA Product Code

• OSM: Hearing Aid, Air Conduction With Wireless Technology

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: 2022-09-19
• Device Publish Date: 2022-09-09

On-Brand Devices [Neosonic]

• 06945936703448: Neosonic BT-Omni
• 06945936703400: Neosonic MX-Smart
• 06945936703455: Poco X405