"Lacrivera" External aesthetic restoration prosthesis (Non-Sterile) - Taiwan Registration f725e5278777510125ef1f1f19fed177
Access comprehensive regulatory information for "Lacrivera" External aesthetic restoration prosthesis (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f725e5278777510125ef1f1f19fed177 and manufactured by LACRIVERA INC.. The authorized representative in Taiwan is Kangcheng Biomedical Technology Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including LACRIVERA INC., and 1 recent registrations in the same category. 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
f725e5278777510125ef1f1f19fed177
Ministry of Health Medical Device Import No. 017341
DHA09401734101
Product Details
I General and plastic surgical devices
I3800 In vitro cosmetic repair supplement
Imported from abroad
Dates and Status
Dec 27, 2016
Dec 27, 2021
Cancellation Information
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