TheraLight 360 Full Body Wellness

GUDID 06976812430219

Rhein Laser Technologies Co.,Ltd.

Musculoskeletal infrared phototherapy unit, non-wearable

• Primary Device ID: 06976812430219
• NIH Device Record Key: de64e4ea-64e4-4bf3-a535-65706a2d17d1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TheraLight 360 Full Body Wellness
• Version Model Number: THERALIGHT 360
• Company DUNS: 704587822
• Company Name: Rhein Laser Technologies 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: true
• 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	06976812430219 [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: 2026-03-16
• Device Publish Date: 2026-03-06

On-Brand Devices [TheraLight 360 Full Body Wellness]

• 06976812430233: THERALIGHT FIT
• 06976812430226: THERALIGHT 10X
• 06976812430219: THERALIGHT 360