“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.
Device Details
Registration Details
b629f5c6ead28070a6dd3e3a8f719d36
Ministry of Health Medical Device Manufacturing No. 005876
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

