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Silhouette Instalift - Taiwan Registration e559e905653e3f8699c418b0b6ebc8a8

Access comprehensive regulatory information for Silhouette Instalift in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e559e905653e3f8699c418b0b6ebc8a8 and manufactured by Sinclair Pharma U.S. Inc.. The authorized representative in Taiwan is CLOVERS BIOTECHNOLOGY CO., LTD..

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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e559e905653e3f8699c418b0b6ebc8a8
Registration Details
Taiwan FDA Registration: e559e905653e3f8699c418b0b6ebc8a8
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Device Details

Silhouette Instalift
TW: ๅก‘็ซ‹ๆ„›็ซ‹ๆ็ทš
Risk Class 2
MD

Registration Details

e559e905653e3f8699c418b0b6ebc8a8

Ministry of Health Medical Device Import No. 031195

DHA05603119504

Company Information

United States

Product Details

This product is suitable for facial suspension surgery to fix the position of the subcutaneous tissue of the cheek after lifting upwards.

I General and plastic surgical devices

I4493 Surgical sutures for absorbable polysaccharides

Imported from abroad

Dates and Status

Aug 22, 2018

Aug 22, 2028