Clarity

GUDID 06971094537502

Huizhou Jinghao Medical Technology Co., Ltd

Air-conduction hearing aid, in-the-ear

• Primary Device ID: 06971094537502
• NIH Device Record Key: 1abcbdc6-b63e-4d45-8e91-d43d17311829
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Clarity
• Version Model Number: JH-DW3F
• Company DUNS: 547508199
• Company Name: Huizhou Jinghao Medical Technology Co., Ltd
• Device Count: 1
• 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	06971094537502 [Primary]

FDA Product Code

• QUH: Self-Fitting Air-Conduction Hearing Aid, Over The Counter

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: 2024-03-26
• Device Publish Date: 2024-03-18

Devices Manufactured by Huizhou Jinghao Medical Technology Co., Ltd

• 06971094539483 - JINGHAO: 2025-12-16
• 16971094538506 - Nacenacy: 2025-12-09
• 16971094538513 - Nacenacy Villear: 2025-12-09
• 06971094539452 - JINGHAO: 2025-10-02
• 06971094538431 - Soundure: 2025-09-23
• 06971094538448 - Soundure: 2025-09-23
• 06971094538455 - Soundure: 2025-09-23
• 06971094538424 - BATSTRKS: 2025-09-09