"Nefer" biosynthetic fiber membrane - Taiwan Registration f820d43ee3aa0a443046da50dec262d3
Access comprehensive regulatory information for "Nefer" biosynthetic fiber membrane in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f820d43ee3aa0a443046da50dec262d3 and manufactured by Oriental Innovation Development Co., Ltd. Biomedical Factory. The authorized representative in Taiwan is Nefeier Biomedical Co., Ltd.
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.
Device Details
Product Details
For details, it is Chinese approved copy of the imitation order
I General, Plastic Surgery and Dermatology
I.4018 ่ฆชๆฐดๆงๅตๅท่ฆ่ๆ
Contract manufacturing;; Domestic
Dates and Status
Jun 03, 2015
Apr 07, 2019
Jun 07, 2022
Cancellation Information
Logged out
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