“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.
Device Details
Registration Details
681210cf90079917bfe14b570a5113e7
Ministry of Health Medical Device Manufacturing No. 007837
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

