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“MEDICORE” Heart Rate Variability Analysis Equipment - Taiwan Registration 4e25efc20ad64b1f5d6aa363ac516937

Access comprehensive regulatory information for “MEDICORE” Heart Rate Variability Analysis Equipment in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4e25efc20ad64b1f5d6aa363ac516937 and manufactured by MEDICORE CO., LTD.. The authorized representative in Taiwan is NEWAED WORLDWIDE PROCUREMENT CONGLOMERATE CORPORATION.

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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4e25efc20ad64b1f5d6aa363ac516937
Registration Details
Taiwan FDA Registration: 4e25efc20ad64b1f5d6aa363ac516937
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Device Details

“MEDICORE” Heart Rate Variability Analysis Equipment
TW: “麥迪科”心律變異分析器
Risk Class 2
MD

Registration Details

4e25efc20ad64b1f5d6aa363ac516937

Ministry of Health Medical Device Import No. 031230

DHA05603123006

Company Information

Korea, Republic of

Product Details

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

E Cardiovascular devices

E2780 Hydraulic, pneumatic or photoelectric plethysmron

Imported from abroad

Dates and Status

Jul 31, 2018

Jul 31, 2028