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BIOMAX Series Irradiance
BIOMAX 300BIOMAX 450BIOMAX 600BIOMAX 900Link To 3rd Party Verified Lab Intensity Testing Here Joules vs. mW/cm2: How To Read These Charts? BIOMAX 9th Generation:
We Are the Clinical Standard in Light Therapy.The PlatinumLED
Difference
For 16+ years, PlatinumLED has been the pioneer and leader of ultra-high power red/NIR therapy lights while delivering a superior solution that is relied upon by more medical professionals and home users worldwide than any other company.
Higher Strength + Advanced Spectrum = Superior Results
Lab Verified 3rd Party Output Testing
Certification
Complete, certified output testing performed by accredited lighting industry standard creators, LightLab International
BIOMAX PRO NANOBIOMAX PRO MIDIBIOMAX PRO GRANDEBIOMAX PRO ULTRABIOMAX 300
BIOMAX 450BIOMAX 600BIOMAX 900SAUNAMAX PROStudioMAXThe Most Trusted Clinical & Personal Light Therapy DevicesWith industry-leading certifications, PlatinumLED ensures every device meets the highest standards for safe, effective light therapy.SHOP NOWFDA Class II Medical Device
FDA Class II Medical Device registration is a process that ensures that a medical device is safe and effective, and that
the organization that produces it can consistently meet the standards of the United States Food and Drug Administration (FDA)
DOCUMENTATION FOR ALL LIGHTSBIOMAX PRO SERIESCanada MDL – Medical Device License
A CanadianMedical Device Licence (MDL)isthe official approval granted by Health Canada allowing manufacturers to sell or import Class II, III, or IV medical devices. It verifies that the product meets strict safety, quality, and effectiveness standards.
DOCUMENTATION FOR ALL LIGHTSLab Verified 3rd Party Output Testing
Certification
Complete, certified output testing performed by accredited lighting industry standard creators, LightLab International
BIOMAX PRO NANOBIOMAX PRO MIDIBIOMAX PRO GRANDEBIOMAX PRO ULTRABIOMAX 300BIOMAX 450BIOMAX 600BIOMAX 900SAUNAMAX PROStudioMAXElectrical Testing Laboratories
Certification
ETL certification, or the ETL Listed Mark, is a product safety certification that indicates a product meets North American safety standards. ETL stands for Electrical Testing Laboratories, and the certification is issued by Intertek, an international certification organization.
ANSI/AAMI ES60601-1:2005+A1;A2 - Medical Electrical Equipment - Part 1: General Requirements for Basic Safety and Essential Performance.
IEC 60601-1-6:2010 Ed.3+A1;A2 - Medical Electrical Equipment – Part 1-6: General Requirements for Basic Safety and Essential Performance - Collateral Standard: Usability.
CSA C22.2#60601-1-6:2011 Ed.3+A1;A2 - Medical Electrical Equipment - Part 1-6: General Requirements for Basic Safety and Essential Performance - Collateral Standard: Usability.
IEC 60601-2-57:2011 Ed.1 - Medical Electrical Equipment - Part 2-57: Particular Requirements For The Basic Safety And Essential Performance Of Non-Laser Light Source Equipment Intended For Therapeutic, Diagnostic, Monitoring And Cosmetic/Aesthetic Use.
CSA C22.2#60601-2-57:2011 Ed.1 - Medical Electrical Equipment – Part 2–57: Particular Requirements for the Basic Safety and Essential Performance of Non-Laser Light Source Equipment Intended for Therapeutic, Diagnostic, Monitoring and Cosmetic/Aesthetic Use.
