Precision Flow® Heliox Unit - ARCSA Registration 52acd1096c1e87cdfba28d9449320672

Access comprehensive regulatory information for Precision Flow® Heliox Unit in the Ecuador medical device market through Pure Global AI's free database. This II medical device is registered under ARCSA ID 52acd1096c1e87cdfba28d9449320672 and manufactured by VAPOTHERM INC.. The device was registered on November 12, 2020.

This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Ecuador ARCSA medical device database. Pure Global AI offers free access to Ecuador's complete medical device registry.