Macrolane VRF 30 - Taiwan Registration 7f4a27e94798a1b058b65af145b59d93

Access comprehensive regulatory information for Macrolane VRF 30 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 7f4a27e94798a1b058b65af145b59d93 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.