Dermalux 1000053

GUDID 50607624600286

The Dermalux® Flex MD is a Medical Device for use on a treatment bed/surface. The device emits specific wavelengths of low level, narrow band light for the treatment of certain cosmetic, dermatological and medical indications. The wavelengths used in the Dermalux® Flex MD system are Blue 415nm, Red 633nm and Near Infrared 830nm.

AESTHETIC TECHNOLOGY LTD

Blue/red/infrared phototherapy lamp

• Primary Device ID: 50607624600286
• NIH Device Record Key: 876c0ecb-81d8-4c53-8c94-5fc7d245dc30
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dermalux
• Version Model Number: Flex MD
• Catalog Number: 1000053
• Company DUNS: 218753736
• Company Name: AESTHETIC TECHNOLOGY LTD
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	50607624600286 [Primary]

FDA Product Code

• GEX: Powered Laser Surgical Instrument

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: 2025-09-10
• Device Publish Date: 2025-09-02

On-Brand Devices [Dermalux]

• 50607624600804: The Dermalux® Flex MD is a Medical Device for use on a treatment bed/surface. The device emits
• 50607624600286: The Dermalux® Flex MD is a Medical Device for use on a treatment bed/surface. The device emits
• 50607624600118: 4-Pod LED phototherapy device.