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“Merit” InQwire AMPLATZ Guide Wires - Taiwan Registration 2f0ef50f3cdd76d91c8a7f569b47dbf1

Access comprehensive regulatory information for “Merit” InQwire AMPLATZ Guide Wires in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2f0ef50f3cdd76d91c8a7f569b47dbf1 and manufactured by MERIT MEDICAL IRELAND LIMITED. The authorized representative in Taiwan is Merit Medical Asia 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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2f0ef50f3cdd76d91c8a7f569b47dbf1
Registration Details
Taiwan FDA Registration: 2f0ef50f3cdd76d91c8a7f569b47dbf1
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Device Details

“Merit” InQwire AMPLATZ Guide Wires
TW: “美瑞特”安普拉斯導引導線
Risk Class 2
MD

Registration Details

2f0ef50f3cdd76d91c8a7f569b47dbf1

Ministry of Health Medical Device Import No. 033317

DHA05603331702

Company Information

Product Details

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

E Cardiovascular devices

E1330 Catheter Lead

Imported from abroad

Dates and Status

Mar 13, 2020

Mar 13, 2025