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“NISSEI” Fingertip Pulse Oximeter - Taiwan Registration 539061fbd856fd772233d42f72043b46

Access comprehensive regulatory information for “NISSEI” 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 539061fbd856fd772233d42f72043b46 and manufactured by NIHON SEIMITSU SOKKI CO., LTD., KOMOCHI FACTORY. The authorized representative in Taiwan is SUN-UP HEALTHCARE 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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539061fbd856fd772233d42f72043b46
Registration Details
Taiwan FDA Registration: 539061fbd856fd772233d42f72043b46
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Device Details

“NISSEI” Fingertip Pulse Oximeter
TW: “日本精密”手指型血氧濃度計
Risk Class 2
MD

Registration Details

539061fbd856fd772233d42f72043b46

Ministry of Health Medical Device Import No. 035045

DHA05603504505

Company Information

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E2700 Oximeter

Imported from abroad

Dates and Status

Dec 01, 2021

Dec 01, 2026