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“BISTOS” PATIENT MONITER SYSTEM - Taiwan Registration d24772ca9e2e1d5f069d3dad802cdcd5

Access comprehensive regulatory information for “BISTOS” PATIENT MONITER SYSTEM in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d24772ca9e2e1d5f069d3dad802cdcd5 and manufactured by BISTOS CO., LTD.. The authorized representative in Taiwan is Yu Yi Medical International 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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d24772ca9e2e1d5f069d3dad802cdcd5
Registration Details
Taiwan FDA Registration: d24772ca9e2e1d5f069d3dad802cdcd5
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Device Details

“BISTOS” PATIENT MONITER SYSTEM
TW: “宇益必思妥”生理監視器系統
Risk Class 2
MD

Registration Details

d24772ca9e2e1d5f069d3dad802cdcd5

Ministry of Health Medical Device Import No. 034326

DHA05603432608

Company Information

Korea, Republic of

Product Details

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

E Cardiovascular devices

E2300 Cardiac Monitor (incl. Cardiac Counter and Heart Rate Alert)

Imported from abroad

Dates and Status

Feb 05, 2021

Feb 05, 2026