Restylane Kysse - Taiwan Registration 7b9c1ecb53b86ab60521f408ae21bd98

Access comprehensive regulatory information for Restylane Kysse in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 7b9c1ecb53b86ab60521f408ae21bd98 and manufactured by Q-MED AB. The authorized representative in Taiwan is GALDERMA HONG KONG LIMITED, TAIWAN BRANCH.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.