"Wacoal" in vitro prosthesis (unsterilized) - Taiwan Registration fb0e00889eab3c4df9750955aab3e9f9
Access comprehensive regulatory information for "Wacoal" 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 fb0e00889eab3c4df9750955aab3e9f9 and manufactured by TRULIFE. The authorized representative in Taiwan is TAIWAN WACOAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including TRULIFE, WACOAL CORP., and 2 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
Product Details
Limited to the classification and grading management of medical equipment, in vitro cosmetic repair supplement (I.3800) first level identification range.
I General, Plastic Surgery and Dermatology
I.3800 Repair supplement for cosmetic use in the body
import
Dates and Status
Oct 01, 2021
Oct 31, 2025