Lumen MD 602009

GUDID 00858935006372

Lumen MD Foot and Hand Pad System

HEALTHLIGHT LLC

Musculoskeletal infrared phototherapy unit, non-wearable

• Primary Device ID: 00858935006372
• NIH Device Record Key: db0ccc07-08af-4738-ae1d-6879375814b1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lumen MD
• Version Model Number: LM-CP-S
• Catalog Number: 602009
• Company DUNS: 080183509
• Company Name: HEALTHLIGHT LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: 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: true

Customer Support Contacts

• Phone: 224-234-0342
• Email: customerservice@healthlightllc.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00858935006372 [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: 2018-06-22
• Device Publish Date: 2018-05-22

On-Brand Devices [Lumen MD]

• 00858935006372: Lumen MD Foot and Hand Pad System
• 00858935006358: Lumen MD Dual Foot and Ankle System
• 00858935006341: Lumen MD Foot and Ankle Pad System