Restylane Refyne - Taiwan Registration 078a1d7080246ba486ffc6ed93699d34
Access comprehensive regulatory information for Restylane Refyne in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 078a1d7080246ba486ffc6ed93699d34 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.
Device Details
Registration Details
078a1d7080246ba486ffc6ed93699d34
Ministry of Health Medical Device Import No. 030309
DHA05603030901
Product Details
This product can be used to enhance the fullness of facial tissues. Recommended for the correction of moderate wrinkles such as nasolabial folds, depending on the area and tissue support to be treated, this product should be injected into the middle to deep dermis or subcutaneous tissue. Lidocaine is added to the product to reduce pain during therapeutic injections.
I General and plastic surgical devices
I0007 Hyaluronic acid implants
Imported from abroad
Dates and Status
Jan 04, 2018
Jan 04, 2028

