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Medical Device Registration in Cambodia

Ministry of Health: 

Ministry of Health

Regulatory Authority:       

Department of Drugs and Food (DDF)

Medical Device Regulation:

ASEAN Medical Device Directive (AMDD)

Official Language:   



Class A, B, C and D

Registration Process:     

  • Determine the classification of the device
  • Appoint a local representative
  • Prepare application and Technical File
  • Make the fee payment.
  • Once approved, the manufacturer may market your device.

Documents Required:      

  • Executive Summary
  • Relevant Essential Principles
  • Declaration of Conformity
  • Device Description
  • Summary of Design Verification and Validation
  • Device Labelling

Post-market surveillance: 

Serious threat to public health – 48 hours

Death or serious deterioration in health – 10 days

An event where recurrence might lead to death – 30 days

Legalized/Notarised Documents (if any) 

Declaration of Conformity (DoC)

Applicable QMS:   

ISO 13485

Registration Timeline:      

6 – 12 months

Authorized Representative:        

Yes. Local Representative.

License Validity:     

3 years

Special Notes:       

Labelling should be in local language, Khymer.

Want to know more about this registration process?