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“Allergan” Juvederm Ultra Plus XC - Taiwan Registration 2008b3748869bc477137fbf9d25ebe31

Access comprehensive regulatory information for “Allergan” Juvederm Ultra Plus XC in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 2008b3748869bc477137fbf9d25ebe31 and manufactured by ALLERGAN. The authorized representative in Taiwan is ALLERGAN PHARMACEUTICALS TAIWAN 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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2008b3748869bc477137fbf9d25ebe31
Registration Details
Taiwan FDA Registration: 2008b3748869bc477137fbf9d25ebe31
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Device Details

“Allergan” Juvederm Ultra Plus XC
TW: “愛力根”喬雅登極緻(含利多卡因)
Risk Class 3
MD

Registration Details

2008b3748869bc477137fbf9d25ebe31

Department of Health Medical Device Import No. 021789

DHA00602178908

Company Information

France

Product Details

Juvéderm ULTRA PLUS XC is an injectable implant that fills moderate and/or severe wrinkles in the skin by injecting into the middle and/or deep dermis. This product contains Lidocaine, which can reduce pain during treatment.

I General and plastic surgical devices

Imported from abroad

Dates and Status

Nov 30, 2010

Nov 30, 2025