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“Leadtek” Fingertip Pulse Oximeter - Taiwan Registration 681210cf90079917bfe14b570a5113e7

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 681210cf90079917bfe14b570a5113e7 and manufactured by LEADTEK RESEARCH, INC.. The authorized representative in Taiwan is LEADTEK RESEARCH, INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Litai Technology Co., Ltd. Zhonghe Second Factory, 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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681210cf90079917bfe14b570a5113e7
Registration Details
Taiwan FDA Registration: 681210cf90079917bfe14b570a5113e7
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Device Details

“Leadtek” Fingertip Pulse Oximeter
TW: “麗臺” 手指型脈搏血氧濃度計
Risk Class 2
MD

Registration Details

681210cf90079917bfe14b570a5113e7

Ministry of Health Medical Device Manufacturing No. 007837

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E2700 Oximeter

Produced in Taiwan, China

Dates and Status

Mar 31, 2023

Mar 31, 2028

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