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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.

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078a1d7080246ba486ffc6ed93699d34
Registration Details
Taiwan FDA Registration: 078a1d7080246ba486ffc6ed93699d34
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Device Details

Restylane Refyne
TW: ็‘ž็ตฒๆœ—-ๆ™ถ้‡‡(ๅซๅˆฉๅคšๅกๅ› )
Risk Class 3
MD

Registration Details

078a1d7080246ba486ffc6ed93699d34

Ministry of Health Medical Device Import No. 030309

DHA05603030901

Company Information

Sweden

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