"Chu Laifu" in vitro prosthesis (unsterilized) - Taiwan Registration fba1328ebd42f16e21da2625ecacca17
Access comprehensive regulatory information for "Chu Laifu" in vitro prosthesis (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fba1328ebd42f16e21da2625ecacca17 and manufactured by TRULIFE. The authorized representative in Taiwan is JE CHEENG INDUSTRAL CO., LTD..
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Device Details
Product Details
Limited to the first level recognition range of medical equipment management measures for in vitro cosmetic repair supplements (I.3800).
I General, Plastic Surgery and Dermatology
I.3800 Repair supplement for cosmetic use in the body
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Dates and Status
Sep 20, 2010
Sep 20, 2015
Apr 25, 2018
Cancellation Information
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