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“MicroPort” EasyFinder Diagnostic Catheter - Taiwan Registration df655c413499f8f15121f50b80e3fb8b

Access comprehensive regulatory information for “MicroPort” EasyFinder Diagnostic Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number df655c413499f8f15121f50b80e3fb8b and manufactured by SHANGHAI MICROPORT EP MEDTECH CO, LTD.. The authorized representative in Taiwan is IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG).

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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Registration Details
Taiwan FDA Registration: df655c413499f8f15121f50b80e3fb8b
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Device Details

“MicroPort” EasyFinder Diagnostic Catheter
TW: “微創電生理”診斷導管
Risk Class 2
MD

Registration Details

df655c413499f8f15121f50b80e3fb8b

Ministry of Health Medical Device Land Transport No. 000900

DHA09200090006

Product Details

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

E Cardiovascular devices

E1220 electrode recording catheter or electrode recording probe

Imported from abroad

Dates and Status

Apr 22, 2018

Apr 22, 2023