Vielight Relief

GUDID 00196852718429

Vielight Inc

Red/infrared light phototherapy unit

• Primary Device ID: 00196852718429
• NIH Device Record Key: decc6c2a-76ac-4be7-9e1f-9f2651b5d889
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vielight Relief
• Version Model Number: RLF
• Company DUNS: 202888269
• Company Name: Vielight Inc
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00196852718429 [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: 2024-06-10
• Device Publish Date: 2024-06-01

On-Brand Devices [Vielight Relief]

• 00196852718429: RLF
• 00860009931619: RLF