3W Profi Diodenlaser
Item: PRO3WDIUS
Available now!

Shipping time: 3 - 4 workdays

starting from 17561,65 CHF Old price: 19289,04 CHF

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Studio Profi Diodenlaser 3W

Professionell Hair Removal
Typ Skin I - VI

 

Handstück-Leistung: 1500 Watt
Sehr großer Spot: 15 x 25 mm²
3 Wellenlängen: 755 nm + 808 nm + 1064 nm
Schnelle Arbeitsgeschwindigkeit bis 20 Hz Frequenz

Color
Wave
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Hair Removal

For many women and men, depilation of the body is an integral part of body hygiene and well-being. There are many possibilities, but these methods are usually painful and cause inflammation or redness. In addition, the hairs grow back quickly so that the procedure has to be repeated permanently. Our device frees you permanently from stubble, redness and ingrown hair. Our devices proceed sensitively and with great care during the treatment. The treatment with our devices is gentle and especially gentle on your skin. We offer state-of-the-art technology and much more.

Gentle hair removal is easier than ever before with this diode laser. The diode laser fulfils all criteria to be allowed to play in the upper league. Many people shave themselves daily on difficult body parts or grow and pluck themselves with much effort to the desired result. The effect on longer time however one does not reach completely certainly thereby, but exactly for it this fantastische diode laser was conceived particularly. By the way, pain is a thing of the past with this procedure. The flexible handling was almost perfected by the light construction.


Diode lasers for gentle treatment
The gentle and highly effective process works with a light in the red wave range, which in turn is converted into pure energy. It is possible to work selectively and also extensively. By treating the hair roots, the long-lasting effect is intensified. With an exact wavelength of up to 808 nm, the diode laser is optimally equipped. To be more precise, the thermal development ensures that the hair is deserted. The surrounding tissue is not damaged. All skin types and hair types can be treated.

 

Why buy a diode laser?
The right equipment often determines the success or failure of a service provider. This sophisticated piece of technology outshines several other diode lasers in its class when it comes to important issues such as handling and flexibility that are important for comfort. Your customers will thank you by coming to your store. Our experience so far and the feedback from our customers has been very positive.


What is the difference to other hair removal methods?
A real diode laser differs from other application methods (like the classic IPL) by a highly developed light source. This source is simply called a diode in the technical language used. According to developers, a good diode in a diode laser should be able to be used with constant power. The laser light from the diode laser operates at an optimized wavelength (808 NM), which is why it is often used for hair removal.


Diode laser 2020: The new technology with 3 wavelengths
The wavelength used and the pulse energy used ensure optimal results within an average of 3-6 treatments. The sliding method used here ensures painless treatment and long-lasting results. A modern menu as well as a rather compact handpiece make the diode laser relatively easy to use. The treatment will be pleasantly quiet and quiet for your customers, which of course further increases the comfort. And the more relaxed your customer is, the more customer loyalty will be promoted and maintained.

 


Diode laser hair removal 808 System, use special laser with long Pulse-Width 808nm, can penetrate to hair follicle. Using selective light absorption theory, laser can be preferentially absorbed by the melanin of the hair and then heating the hair shaft and hair follicle, moreover to destroy the hair follicle and oxygen organization around hair follicle. When laser outputs, system with special cooling technology, cool the skin and protect skin from being hurt and reach a very safe and comfortable treatment!
In the crowded field of energy-based hair removal systems, IPL Swiss Premium stands out of the competition by offering cutting edge technology for effective fast and viryually painless treatments.


ADVANTAGES

Europe Medical CE and US FDA Approved
The Lightest handpiece: 375g, superior to others(=800g) in the market.

The Highest Power: 1500W Energy density is 3 times higher, comparable to world’s top equipment
The Biggest Spot Size: 15*25mm

Produced in the US
-5 Grad Sapphire cooling
20 million shots guaranteed
Superior Semi-conductor cooling, 24 hours continuous working.
High cost performance equipment, available for 10 years.

Super Großer Spot


The 3 wavelengths :

Alex 755 nm Wavelength
Low penetration depth compared to other methods. Wavelength more suitable for fine and light hair. Suitable for various hair types and colours. The so-called Alexandrite wavelength offers a stronger energy absorption.

Speed 808 nm Wavelength
Mean penetration depth. The classic wavelength of hair removal devices. Half treatment time on average. Classic wavelengths in professional laser hair removal, the 808 nm wavelength.

Yag 1064 nm Wavelength
High penetration depth in comparison. Wavelength for darker skin and deep hair. The wavelength Yag 1064 is characterized by a lower melanin absorption and is therefore a focused solution for darker skin types. Especially for darker skin types.

 

Our seals of approval, approvals and guarantee

Our devices are subject to the highest safety standards and have worldwide
Approvals, for safe operation.

U. S. Food and Drug Administration

The FDA (Food and Drug Administration) in the USA is the only official federal authority in the world that has laser and IPL devices tested for their effectiveness for permanent hair reduction at the request of the manufacturer (510(k) approval).

To be allowed to work with a device in the USA, it must have the "normal" FDA approval. Similar to the CE certification in the EU, the device is tested for safety and harmlessness. All devices on the US market have this FDA seal.

The FDA does not differentiate between lasers and IPL devices in the approval process. For simplicity, both types of devices fall under the existing category of dermatological and surgical lasers class 2 (CFR 878.4810). In official statements of the FDA, only lasers are mentioned although IPL is also included.

TÜV Süd

The road to the various markets is paved with extremely strict requirements, especially in the medical products sector: the products must meet the highest quality standards and their quality management must be designed accordingly. Here it is sensible and good to be able to consult an experienced expert. Just like TÜV SÜD. We have been testing and certifying quality management for medical devices for over 30 years and have the necessary know-how, not least thanks to the continuous training of our specialists. This is why we are among the market leaders in countries with strict regulation of medical devices and count many leading manufacturers among our customers. Our quality management certificates confirm that we comply with a whole range of international standards - most notably ISO 13485, which means that you as a manufacturer have proof that certified quality management has been applied in the manufacture of your medical devices and that it meets the highest requirements. This promotes your image as a manufacturer, strengthens the confidence of authorities, buyers and users in your products and provides clear sales arguments.

ISO 13485

Companies that develop and manufacture medical devices ensure the marketing and manufacturing processes by means of a comprehensive quality management system in accordance with ISO 13485. The basis is that for medical devices that are established on the German market, regulations and legal requirements must be observed: Medizinproduktegesetz (MPG), which together with its ordinances implements the European Directives 90/385/EEC (for active implants), 93/42/EEC (for other medical devices) and 98/79/EC (for in-vitro diagnostics) in Germany. The EN ISO 13485 standard describes the specific requirements for quality management systems in the medical device industry. Added to this is the position in EN ISO 9001 and other industry-specific conditions for medical devices.

Although ISO 13485 is an independent document, the requirements are largely identical to those of ISO 9001, which focuses on the requirement that companies/organizations must strive for continuous optimization under quality management aspects. ISO 13485 focuses on product safety. It is important to ensure that the efficiency of the implemented processes meets the product requirements.

Medical devices - seal of approval

The EN ISO 13485 standard "Medical devices: Quality management systems - Requirements for regulatory purposes" deals with the requirements that manufacturers and suppliers of medical devices must meet when developing, implementing and maintaining management systems for the medical device industry. Originally developed in the 1990s, the standard contains requirements for quality management systems that meet customer needs as well as regulatory requirements of the European Union (EU), Canada and other major markets worldwide.

EN ISO 13485 is similar in scope and purpose to ISO 9001, but contains additional requirements specific to medical devices and reformulates some of the requirements of ISO 9001. In most markets, ISO 9001 certification is therefore not an adequate substitute for EN ISO 13485 certification.

ECM – Ente Certificazione Macchine

Ente Certificazione Macchine is a well-known body authorized by the European Commission to issue EC certificates in accordance with Directive 93/42/EEC (MDD). [See the ECM accreditations on the database Nando Information System qui of the European Commission].

The CE mark The CE mark is the mandatory certification mark that every medical device must have in order to be marketed and used in the European Union. The CE mark declares that the product complies with the applicable European directives. The Medical Device Directive 93/42/EEC (MDD) lists the basic safety, efficacy and quality requirements that a medical device must meet in order to receive the CE mark and be allowed to be placed on the European market.

EU 765/2008

The CE marking indicates that the machine meets the requirements of the Machinery Directive. This also applies to all other applicable EC directives. Each machine may be provided with exactly one CE mark. The CE marking must stand on an equal footing with the manufacturer's information and be applied using the same technique.

CE stands for Communauté Européenne (European Community). The marking indicates that a product or machine complies with the relevant European directives. The CE mark, introduced in 1995, is therefore to be understood as a "passport" for machines, as it allows machines to be both marketed and operated in the EU. It is important that the CE mark should not be confused with a seal of approval or quality mark.

For further information and questions, please contact us.

Our trainings take place according to manufacturer guidelines and consist of theory and practice. After passing the exam, you will receive a certificate and can therefore legally carry out treatments. Our trainers are trained by the Chamber of Industry and Commerce.

Medical training

Basics and structure of the skin

Basics and structure of hair

different skin types and their reactions

Special fields ( device dependent ) and fields of application

Basics of permanent hair removal

Basics of Acne Treatment

Basics of skin treatment

Basics of vascular treatments

Basics of the treatment of pigment spots

Technical basics / factors ( device dependent )

light

radio frequency

IPL devices

SHR devices

Radio Frequency Devices

treatment implementation

Safety instructions and protective measures

Hygiene and disinfection

treatment process

customer information

Checklists for treatment

Anamnesis questionnaires for the treatment

Technical terms around your devices

Legal forms for treatment

Insurance guidelines

Practical examination

Instruction on the device

treatment stages

care instructions

Our trainings take place in our training center or in your studio. Every year, there is a further training course for you. Every month you will receive treatment tips from us and all information from the manufacturer.

Of course our support is at your disposal to answer all your questions immediately.

Would you like to become self-employed in the field of IPL treatments? Then you are with us completely at the correct address.

We have special offers for start-ups. This includes the media package with the creation of your websites, Facebook and a reservation system for your customers. We guide and familiarise you with the complex areas so that your independence becomes a success right from the start.

 

Financing partner

Since IPL-Swiss works together with various leasing companies, we will find the right leasing partner for you quickly and easily. Just contact us and we will take care of it!

 

IPL Swiss hire purchase
You make a deposit, which varies according to the device and your creditworthiness.
After that you can pay monthly installments to us and start earning money immediately.

 

Of course you get the training also with a installment purchase of the device FREE OF CHARGE!

If you have gained a foothold in the IPL business, YOU will receive a 2nd training with which you can deepen your knowledge.

You will receive a monthly newsletter from us with application tips and tricks from our customers, which are stored in the knowledge database. It contains applications, skin types and all important information - about your device since 7 years.

Of course you will receive the phone number of our emergency team, which is available 7 days a week. Here one will help you immediately.

Interest ? Call us without obligation .

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