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Arazygroup.com - Medical Device Registration in Europe, Please fill the following form and submit your inquiry or discuss it with one of our online specialists. Let\'s get your products registered in Europe!

Medical devices are divided into class I, IIa, IIb and III. IVDs are divided into four categories: General IVDs, self-diagnostics, list A and list B. All medical devices exempt class I and General IVDs require the involvement of a Notified Body and the implementation of a quality management system, usually in line with ISO 13485.

Gain CE Mark approval and fulfill the CE mark requirements with the help of our global experts and team of qualified marketing professionals, regulatory specialists, scientists and the best brains behind achieving product validation for medical device manufacturers and distributors in Europe.

http://www.arazygroup.com/europe - CE Mark consultants for medical device validation, clearance and certification throughout the European Union.

http://www.arazygroup.com - Medical Device Regulatory Services from medical device consultancy experts in North America, Europe, Asia, Africa and Australia.