Mito Red Light Cabin 2.0
Select Options:
$13,495.00
Description
Want to add Red Light Therapy to your home or business, but not sure where to put it?
Want to offer your members access to this amazing modality with ease of use and maximum privacy without having to hide the devices in a closet or build out a whole separate room?
We’ve solved those problems for you!
Key Features
- Commercial Grade Red Light Therapy: Each MitoCABIN 2.0 comes with either one or two MitoPRO Commercial Ultimate X panels, depending on your chosen configuration.
- Minimal Footprint yet feels Spacious: The MitoCABIN 2.0 is 4ft X 5ft deep X 7.5ft tall.
- Easy to Assemble – Requires two people and minimal tools. The panels are designed to sit on the floor, so no hanging of light panels is required!
- Made with Health in Mind: Constructed with VOC-free glue to ensure no off-gassing; the beautiful red cedar is durable and not prone to off-gassing, which is why it is very commonly found in high-quality saunas.
- Electrical: Dedicated 15-amp 120-volt circuits required for each panel.
Included Extras: All purchases come with a small bench, shelf, and our marketing support package ($500+ value), which includes educational brochures, IR glasses, and a large pop-up display banner to help upsell the modality.
Certifications
The MitoCABIN 2.0 meets our high standards and many international standards, both voluntary and mandatory. Here is a full list of the standards that our product is built to.
- ETL – A safety certification for products that meet North American electrical, sanitation, and operational safety standards. Intertek, an independent testing organization, administers it.
- CE – The CE standard is a mark that indicates a product meets European Union (EU) safety, health, and environmental regulations.
- MDSAP – The Medical Device Single Audit Program (MDSAP) is a program that allows third-party auditors to perform a single audit of a medical device manufacturer. The audit covers the manufacturer’s quality management system and regulatory requirements.
- ISO 13485 – Manufactured in a facility that meets ISO international quality standards. Ensuring safety and quality in the design, manufacturing, and installation of medical devices.
- FDA Class II – Our devices are manufactured in a registered FDA Class two manufacturing facility.
$19,995.00
Description
Want to add Red Light Therapy to your home or business, but not sure where to put it?
Want to offer your members access to this amazing modality with ease of use and maximum privacy without having to hide the devices in a closet or build out a whole separate room?
We’ve solved those problems for you!
Key Features
- Commercial Grade Red Light Therapy: Each MitoCABIN 2.0 comes with either one or two MitoPRO Commercial Ultimate X panels, depending on your chosen configuration.
- Minimal Footprint yet feels Spacious: The MitoCABIN 2.0 is 4ft X 5ft deep X 7.5ft tall.
- Easy to Assemble – Requires two people and minimal tools. The panels are designed to sit on the floor, so no hanging of light panels is required!
- Made with Health in Mind: Constructed with VOC-free glue to ensure no off-gassing; the beautiful red cedar is durable and not prone to off-gassing, which is why it is very commonly found in high-quality saunas.
- Electrical: Dedicated 15-amp 120-volt circuits required for each panel.
Included Extras: All purchases come with a small bench, shelf, and our marketing support package ($500+ value), which includes educational brochures, IR glasses, and a large pop-up display banner to help upsell the modality.
Certifications
The MitoCABIN 2.0 meets our high standards and many international standards, both voluntary and mandatory. Here is a full list of the standards that our product is built to.
- ETL – A safety certification for products that meet North American electrical, sanitation, and operational safety standards. Intertek, an independent testing organization, administers it.
- CE – The CE standard is a mark that indicates a product meets European Union (EU) safety, health, and environmental regulations.
- MDSAP – The Medical Device Single Audit Program (MDSAP) is a program that allows third-party auditors to perform a single audit of a medical device manufacturer. The audit covers the manufacturer’s quality management system and regulatory requirements.
- ISO 13485 – Manufactured in a facility that meets ISO international quality standards. Ensuring safety and quality in the design, manufacturing, and installation of medical devices.
- FDA Class II – Our devices are manufactured in a registered FDA Class two manufacturing facility.
How To use
