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“Nipro” Guideplus 2 Guide extension catheter - Taiwan Registration ea91341abeca7fcdd1097b468088263c

Access comprehensive regulatory information for “Nipro” Guideplus 2 Guide extension catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ea91341abeca7fcdd1097b468088263c and manufactured by Nipro Corporation Odate Factory. The authorized representative in Taiwan is LEIN YIH MEDICAL CO..

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ea91341abeca7fcdd1097b468088263c
Registration Details
Taiwan FDA Registration: ea91341abeca7fcdd1097b468088263c
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Device Details

“Nipro” Guideplus 2 Guide extension catheter
TW: “尼普洛”蓋普拉斯第二代導引延長導管
Risk Class 2
MD

Registration Details

ea91341abeca7fcdd1097b468088263c

Ministry of Health Medical Device Import No. 035010

DHA05603501002

Company Information

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular devices

E1250 Percutaneous catheter

Imported from abroad

Dates and Status

Oct 27, 2021

Oct 27, 2026