##  [Successful Identification of Medical Device Category in the EU Region](/case-studies/successful-identification-of-medical-device-category-in-the-eu-region) 

- [Medical Devices](/case-studies-main-categories/medical-devices)
- [Market Access](/case-studies-main-categories/market-access)





[EMA](/case-studies-heath-authority/ema)

 

 ![Successful Identification of Medical Device Category in the EU Region]()

The client is a leading CRO and genome scale diagnostic services company that was looking for assistance with the classification of its NSG technology based medical device in the European region. Freyr supported the client by decoding the classification of the device and its Regulatory requirements for the registration process.

Download the case study to comprehend Freyr’s approach of identifying the classification of the device as per the EU Regulatory requirements.



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