Yihong

GUDID 06975850450012

Shenzhen Yihong Lighting Co., Ltd.

Blue/red/infrared phototherapy lamp

• Primary Device ID: 06975850450012
• NIH Device Record Key: de83b9c7-c21d-404e-b68a-98e648d04bd1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Yihong
• Version Model Number: YD001
• Company DUNS: 710198401
• Company Name: Shenzhen Yihong Lighting 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: false
• Serial Number: true
• Manufacturing Date: false
• 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	06975850450012 [Primary]

FDA Product Code

• ILY: Lamp, Infrared, Therapeutic Heating

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: 2023-02-28
• Device Publish Date: 2023-02-20

Devices Manufactured by Shenzhen Yihong Lighting Co., Ltd.

• 06975850450159 - Cabpay: 2024-10-28
• 06975850450036 - Cabpay: 2024-07-31
• 06975850450562 - Cabpay: 2024-04-16
• 16975850452259 - Cabpay: 2024-04-09
• 16975850450071 - Cabpay: 2023-12-21
• 16975850451016 - Cabpay: 2023-12-12
• 16975850451023 - Cabpay: 2023-12-12
• 16975850451030 - Cabpay: 2023-12-12