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"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.

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f820d43ee3aa0a443046da50dec262d3
Registration Details
Taiwan FDA Registration: f820d43ee3aa0a443046da50dec262d3
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Device Details

"Nefer" biosynthetic fiber membrane
TW: โ€œๅฅˆ่ฒๅ…’โ€็”Ÿ็‰ฉๅˆๆˆ็บ–็ถญ่†œ
Risk Class 2
Cancelled

Registration Details

f820d43ee3aa0a443046da50dec262d3

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

I General, Plastic Surgery and Dermatology

I.4018 ่ฆชๆฐดๆ€งๅ‰ตๅ‚ท่ฆ†่“‹ๆ

Contract manufacturing;; Domestic

Dates and Status

Jun 03, 2015

Apr 07, 2019

Jun 07, 2022

Cancellation Information

Logged out

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