Frequently Asked Questions

Healy devices and most of their components are made in Germany. Research, product development, and supply chain are managed from the head office in Berlin, whereas there is also a further research and development centre in Wiesbaden, Germany. Most of the product supply chain is in Germany, however, some marketing materials and non-medical items such as the Welcome-Video-Brochure are made in China or other countries.

Healy World GmbH deploys a peer to peer direct sales strategy with a central distribution system headquartered in Germany. Device users can register to buy the device and shop for related items online. Some users may wish to become distributors and resellers of the device especially in over 46 countries where Healy is authorised for sale.

Company terms can be found here <Download PDF>

Medical Devices are heavily regulated in Germany to the highest recognised global standards, and as such, Healy devices come with the “CE” mark to indicate compliance and conformity with applicable European regulations. Healy CE 0482

According to European regulatory directives for medical devices, the classification is based on a) duration and b) location of the application of such devices. Healy is classified as a Class II (a) medical device in Europe.

Healy is approved with the US Food & Drugs Administration (FDA) as a Class II medical device, primarily as a “Transcutaneous electrical nerve stimulator for pain relief“. Further, its indications for use are describes as follows: “The device is designed to be used for temporary relief of pain associated with sore and aching muscles in the shoulder, waist, back, arms and legs due to strain from exercise or normal household work activities and for the symptomatic relief and management of chronic, intractable pain and relief of pain associated with arthritis”. accessdata.fda.gov/cdrh_docs/pdf19/K191075.pdf

 In 1991, Christian Halper co-developed a software system for the technical analysis of financial data that was the foundation of the legendary Superfund Investment Group in Austria who’s success was built on following the hottest trends in the marketplace. Christian has allocated 100 million exclusively for the development and marketing of Healy. A fund manager, before allocating a large sum of investment, can be deemed to have performed sufficient due diligence on the business case, company structure and product viability before making such an investment decision.

Healy is currently authorised for sale in:

Australia, Austria, Belgium, Bulgaria, Cambodia, Croatia, Cyprus, Czech Republic, Denmark, England,

Estonia, Finland, France, Germany, Greece, Hungary, India, Indonesia, Ireland, Italy,

Japan, Laos, Latvia, Lithuania, Luxembourg, Malaysia, Malta, Myanmar, Netherlands, New Zealand,

Norway, Philippines, Poland, Romania, Russia, Slovakia, Slovenia, Spain, Sweden, Thailand,

Ukraine, USA, Vietnam

According to current European Regulations, it is possible to become a Medical Device Advisor which is a facility provided by the company, subject to appropriate training, regulatory documentation and compliance reporting standards established for this purpose. Outside of Europe, distributors and affiliates may set-up as independent business owners and use the company back-office for additional resources such as PDF documents and videos which provide sufficient information for prospective buyers to make an informed decision.

Any Question ?

Please don’t hesitate to contact us with any additional questions you may have about the products at Vital for your Health. We value our customers and will be sure to address your needs and concerns.

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