Redfy

GUDID 16975981280011

SunPlus LED Technology Co., Ltd.

Cosmetic red-light phototherapy system, home-use

• Primary Device ID: 16975981280011
• NIH Device Record Key: 9501ca6e-8a3e-4742-bbe3-413b21c968d6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Redfy
• Version Model Number: RD2000
• Company DUNS: 553358256
• Company Name: SunPlus LED 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: false
• 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	16975981280011 [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: 2023-05-31
• Device Publish Date: 2023-05-23

On-Brand Devices [Redfy]

• 16975981280011: RD2000
• 06975981280014: RD2000