E-One Visit and test tomorrow

So tomorrow I have an appointment to go into Brisbane and see it in the shop.
I had a lovely chat on the phone today from Aurelien the sales manager, after I left a message last night.
It was great to get a phone call and an email.


He was extremely helpful on the phone and allayed my fears that not only is this alot of money, but assured me that this machine in its strength is at least 5 times more powerful than the viss. Which he explained had been tested in France. It seems they test every new home device that comes onto the market to see what it really is like.


This machine comes with a 6 months money back guarantee and a 2 year warranty.


There are lots of helpful video's on the site, and the most positive is the fact that it is made in France, has been tested over 3 years, is the only TGA registered and certified home laser treatment for medical use.
 It is not a cosmetic machine, but the real thing with lots of safety features.


For those just starting to look. here is the link to E-one 

Tomorrow I will let you know if it hurts, and we will see how hubby goes, he is the bigger sook with these things.

TGA registration

France Cosmetic is proud to announce that the E-One is registered  by the Australian Therapeutic Goods Administration for the safe treatment of Hirsutism (excessive hair growth). The device is listed on Australian Register of Theraputic Goods (ARTG) under ref #167727.

International certification

Medical CE - 93/42/ECC
ISO 9001 – 2000
ISO 13485 – 2003

Medical certification

Any device that is available for purchase in Europe is required to bear a CE logo, this logo is verification that the product has been thoroughly tested and is safe to use for the general public.  However, it is unfortunately common to find many companies affixing a CE logo on their own accord to the product without any safety tests.

In Europe, when it comes to devices that are designed to interact with the body, a different kind of CE certification is required: a Medical CE.  The approval process for a Medical CE includes an extra set of requirements compared to the normal CE certification process.  These extra requirements are designed offer the end user an assurance that the product they are using (providing it is used within the recommended guidelines) is completely safe.

A Medical CE can only be issued by approved authorities; these authorities are worldwide, independent, accredited organizations (ie. SGS and Veritas).  Due to the separation of duties, the manufacturer cannot have any influence upon the Medical CE application process.

The E-One hair removal device is the only home-use IPL device in the world to possess a Medical CE mark. The device was able to pass the stringent requirements of a Medical CE due to the high standards adhered to by the manufacturing company. The standards adhered to include ISO 9001 and ISO 13485 and numerous electrical safety tests.

SAFETY STANDARDS

The E-One hair removal device was designed with a total of 12 stages of safety, meaning users have to confirm they are using the device safely. The implementation of these interactive safety precautions enables a higher level of safety in the comfort of your home.

AN OBSESSION WITH QUALITY – ISO 9001 AND 13485

For a company to produce a high quality product, they are required to adhere to the ISO 9001 and ISO 13485 standards. The implementation of these strict rules provides a level of traceability for both the E-One’s individual components and every E-One device sold. A high level of quality control is implemented on every component of the E-One device throughout the manufacturing process, which is followed by an array of stringent tests.

The implementation of these rules does have an impact on the sale price, as France Cosmetic would rather provide a guarantee of the utmost in terms of quality.