The Medical Device Regulation (MDR), known as Regulation 2017/745
Known as Regulation 2017/745, is a regulation governing the marketing and use of medical devices in the European Union. MDR regulates the acquisition of CE certification for medical device manufacturers and imposes strict requirements regarding the safety and effectiveness of products.
Contact and Application
Our company provides CE certification services under the scope of MDR. For application and further information, please use the following contact details:
To access the application form and application instructions, you can visit the "Documents" section on our website.
Don't hesitate to get in touch with us to express your questions, submit your applications, or convey your needs. We are here to assist you with all the requirements related to MDR compliance
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