"Lacrivera" External aesthetic restoration prosthesis (Non-Sterile) - Taiwan Registration 017c8bbd00c309225f960fed3eb9130f
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 017c8bbd00c309225f960fed3eb9130f and manufactured by LACRIVERA INC.. The authorized representative in Taiwan is Kangcheng Biomedical Technology Co., Ltd.
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Device Details
Registration Details
017c8bbd00c309225f960fed3eb9130f
Ministry of Health Medical Device Import Registration No. 017341
DHA08401734105
Product Details
Limited to the first level recognition range of medical equipment management measures for in vitro cosmetic repair supplements (I.3800).
I General and plastic surgical devices
I3800 In vitro cosmetic repair supplement
Imported from abroad
Dates and Status
Oct 01, 2021
Oct 31, 2023