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        Are you planning to invest in a cryolipolysis device, a professional laser hair removal machine, or another cutting-edge aesthetic technology?
In France and across Europe, this certification has become mandatory to operate legally and ensure client safety.
Yet, confusion remains common: many professionals still confuse the simple CE marking (found on a hair dryer or a child’s toy) with the CE Medical certification, which is reserved for medical and medical-grade aesthetic devices.
So, what exactly does this marking mean?
Since when has it been required?
And why is it a true guarantee of credibility, safety, and profitability for your business?
Here’s everything you need to know.
The CE (Conformité Européenne) marking was introduced in 1993 to harmonize safety standards within the European Union.
But not all CE markings mean the same thing:
Standard CE → applies to consumer goods (appliances, toys, electronics).
CE Medical → applies to medical and paramedical devices, including aesthetic technologies with a medical purpose (laser hair removal, IPL, cryolipolysis, radiofrequency, HIFU, etc.).
The CE Medical marking proves that the device has undergone rigorous testing, evaluation, and validation according to strict European safety and performance standards.
Since May 2021, Regulation (EU) 2017/745 — known as MDR (Medical Device Regulation) — has made CE Medical certification mandatory for all aesthetic devices with a medical purpose in order to be marketed or used legally.
Devices already in circulation before 2021 are under a transitional period, but starting in 2029, no device will be legally usable without CE Medical certification.
???? See the official text on Legifrance
Earning CE Medical certification is a demanding and highly regulated process — long, complex, and costly.
A manufacturer must demonstrate full compliance through:
Clinical and technical trials proving safety and efficacy
Strict traceability of all components
Detailed regulatory documentation validated by notified bodies
Regular audits by independent experts
In practice, obtaining CE Medical certification can take several years and requires collaboration between engineers, doctors, and regulatory specialists.
At Contour Paris, we know this process inside and out: all our technologies, including the Clinical Skin Laser, have successfully passed every stage of this stringent certification journey.
Why is it so important to invest in a CE Medical certified device?
Because it directly impacts your clients’ safety, your legal security, and your brand reputation.
A CE Medical certified laser or cryolipolysis device is designed to minimize risks such as burns, scarring, pain, or hyperpigmentation.
Your clients feel safe — and that confidence keeps them coming back.
CE Medical ensures that you work with:
Reliable, ergonomic devices
Validated components
Fewer breakdowns and unexpected issues
Using certified equipment is also a powerful marketing argument.
It proves that you offer safe, regulated treatments — strengthening your reputation and boosting client trust, leading to a faster return on investment.
Unfortunately, the market is full of imported, low-cost machines sold as “innovative” — but lacking CE Medical certification.
Here’s what you risk:
Illegality: Their use is banned in France. In case of inspection or injury, you are fully liable.
Safety hazards: Burns, scarring, infections — serious consequences for both your clients and your reputation.
Financial loss: Unreliable equipment, frequent breakdowns, and loss of client trust threaten your profitability.
Pro tip: Always ask for the official CE Medical certificate before purchasing.
If the supplier can’t provide it — walk away.
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