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“Leadtek” Fingertip Pulse Oximeter - Taiwan Registration b629f5c6ead28070a6dd3e3a8f719d36

Access comprehensive regulatory information for “Leadtek” Fingertip 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 b629f5c6ead28070a6dd3e3a8f719d36 and manufactured by Litai Technology Co., Ltd. Zhonghe Second Factory. The authorized representative in Taiwan is LEADTEK RESEARCH, INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including LEADTEK RESEARCH, INC., and 1 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.

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b629f5c6ead28070a6dd3e3a8f719d36
Registration Details
Taiwan FDA Registration: b629f5c6ead28070a6dd3e3a8f719d36
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Device Details

“Leadtek” Fingertip Pulse Oximeter
TW: “麗臺” 指尖式脈搏血氧儀
Risk Class 2
MD

Registration Details

b629f5c6ead28070a6dd3e3a8f719d36

Ministry of Health Medical Device Manufacturing No. 005876

Company Information

Taiwan, Province of China

Product Details

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

E Cardiovascular devices

E2700 Oximeter

Produced in Taiwan, China

Dates and Status

Sep 26, 2017

Sep 26, 2027

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