SculptIris Laser Bodyforming 1060 nm
... is the first non-invasive body slimming with
SculptIris is the world's first FDA-approved technology laser treatment for non-invasive lipolysis of the abdomen,
flanks, back, inner thighs, outer thighs and is now available for the submental area (under the chin).
It is designed to safely and effectively eliminate unwanted fat cells.
The result is permanent reduction of stubborn fat without surgery or downtime.
-Minimal absorption in the dermis leaves the skin surface intact.
-Advanced contact cooling increases patient comfort
-Feather-light heat distribution provides natural-looking results
-Fast, 25-minute treatment per area
-Flat, suction-free applicator design for even and natural-looking results
-Simple and efficient attachment system
-Non-invasive, customized treatments for your clients
-No surgery, no downtime
-flat, non-absorbent applicator design for even, natural-looking results
-Non-invasive, customized treatments for your patients
-Simple and efficient attachment system
The specific affinity of the 1060 nm wavelength for adipose tissue, coupled with minimal absorption in the dermis
allows SculptIris to efficiently treat areas of troublesome fat in as little as 25 minutes.
The body naturally eliminates the destroyed fat cells, with results visible in as little as 6 weeks
and optimal results are typically seen in as little as 12 weeks.
|Pulse Length||1s - 20s|
|Work time||25 Minutes|
|Applicator size||55 x 105 mm|
|Treatment clamp indicating light||Red (630nm)/Green(570nm)/50mW×4|
|Working Temperature||5 Grad~30 Grad|
|Package Size||120*62*60mm & 60*46*19mm|
|Rated Input Power||AC110V/60Hz AC220V/50Hz|
|Maximum Input Power||2500W|
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.
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.
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.
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.
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 )
Radio Frequency Devices
Safety instructions and protective measures
Hygiene and disinfection
Checklists for treatment
Anamnesis questionnaires for the treatment
Technical terms around your devices
Legal forms for treatment
Instruction on the device
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.
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 .