ECUADOR
General country-specific regulatory information is provided on this page. Become a LICENSALE.COM user to receive detailed device-specific compliance information for each market, free of charge, to expedite the preparation of your medical device or IVD registration application.

REGULATORY AUTHORITY
: Medical devices are regulated by the ARCSA or Agencia Nacional de Regulación, Control y Vigilancia Sanitaria (National Health Regulation, Control, and Surveillance Agency). 

CLASSIFICATION SYSTEM: Medical devices are classified according to the EU risk-based model into Classes I, IIa, IIb, III, and IV.

TIMEFRAME: As regulations in Ecuador are new, the timeframe for approval is uncertain. However, it is estimated that the process takes about three weeks for preliminary review with an additional 15 working days to review the hard copy submission.

AUTHORIZED REPRESENTATIVE: An authorized representative is required to register medical devices in Ecuador.

Last updated on March 17 2015.



Interested in obtaining fast market approval for your medical device or IVD in Ecuador? REQUEST A FREE QUOTE>

For more information on registration in Ecuador, check out the following articles on our blog:
Country at a Glance: Ecuador
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