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"Baijie" finger pulse oximeter - Taiwan Registration 71c8d636e5fb062425dbac20fb13307e

Access comprehensive regulatory information for "Baijie" finger pulse oximeter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 71c8d636e5fb062425dbac20fb13307e and manufactured by Baichen Technology Co., Ltd. The authorized representative in Taiwan is VIA-TECH 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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71c8d636e5fb062425dbac20fb13307e
Registration Details
Taiwan FDA Registration: 71c8d636e5fb062425dbac20fb13307e
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Device Details

"Baijie" finger pulse oximeter
TW: โ€œ็™พๆทโ€ๆ‰‹ๆŒ‡ๅž‹่„ˆๆ่ก€ๆฐงๅ„€
Risk Class 2

Registration Details

71c8d636e5fb062425dbac20fb13307e

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.2700.

Contract manufacturing;; Domestic

Dates and Status

Dec 01, 2022

Dec 01, 2027