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“OMRON” Automatic Blood Pressure Monitor - Taiwan Registration 96f8807488a873b2f323f3a12b88c1e3

Access comprehensive regulatory information for “OMRON” Automatic Blood Pressure Monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 96f8807488a873b2f323f3a12b88c1e3 and manufactured by For use only by the Parts System Denda;;OMRON HEALTHCARE CO., LTD. MATSUSAKA FACTORY. The authorized representative in Taiwan is OMRON HEALTHCARE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including OMRON HEALTHCARE CO., LTD. MATSUSAKA FACTORY, OMRON HEALTHCARE MANUFACTURING VIETNAM CO., LTD., and 5 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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96f8807488a873b2f323f3a12b88c1e3
Registration Details
Taiwan FDA Registration: 96f8807488a873b2f323f3a12b88c1e3
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Device Details

“OMRON” Automatic Blood Pressure Monitor
TW: “歐姆龍”電子血壓計
Risk Class 2
MD

Registration Details

96f8807488a873b2f323f3a12b88c1e3

Ministry of Health Medical Device Import No. 025833

DHA05602583301

Product Details

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

E Cardiovascular devices

E1130 Non-invasive blood pressure measurement system

Imported from abroad

Dates and Status

Mar 07, 2014

Mar 07, 2024

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