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“ASTERASYS” Liftera-V high intensity focused ultrasound surgical unit - Taiwan Registration f97fe977e3527032ca6ba73873b3155c

Access comprehensive regulatory information for “ASTERASYS” Liftera-V high intensity focused ultrasound surgical unit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f97fe977e3527032ca6ba73873b3155c and manufactured by ASTERASYS Co., Ltd.. The authorized representative in Taiwan is BP BIOTECHNOLOGY COMPANY.

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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f97fe977e3527032ca6ba73873b3155c
Registration Details
Taiwan FDA Registration: f97fe977e3527032ca6ba73873b3155c
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Device Details

“ASTERASYS” Liftera-V high intensity focused ultrasound surgical unit
TW: “艾特拉喜”立特拉聚焦超音波
Risk Class 2
MD

Registration Details

f97fe977e3527032ca6ba73873b3155c

Ministry of Health Medical Device Import No. 034711

DHA05603471101

Company Information

Korea, Republic of

Product Details

Details are as detailed as approved Chinese instructions

I General and plastic surgical devices

I4590 Focused Ultrasound Stimulator

Imported from abroad

Dates and Status

Jul 17, 2021

Jul 17, 2026