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“Pasesa” Non-invasive Vascular Screening Device - Taiwan Registration 2016e2029f2779d03fcefc57464e71e0

Access comprehensive regulatory information for “Pasesa” Non-invasive Vascular Screening Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2016e2029f2779d03fcefc57464e71e0 and manufactured by SINTAI OPTICAL(SHEN ZHEN)CO., LTD.. The authorized representative in Taiwan is GENEWAY 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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2016e2029f2779d03fcefc57464e71e0
Registration Details
Taiwan FDA Registration: 2016e2029f2779d03fcefc57464e71e0
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Device Details

“Pasesa” Non-invasive Vascular Screening Device
TW: “帕醫生”非侵入性血管檢測儀
Risk Class 2
MD

Registration Details

2016e2029f2779d03fcefc57464e71e0

Ministry of Health Medical Device Land Transport No. 001193

DHA09200119302

Company Information

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; Made in China

Dates and Status

Jan 06, 2021

Jan 06, 2026