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“Merit” SPLASHWire Hydrophilic Guide Wire - Taiwan Registration 60663ff73efb62bf8ab5b73d117f30b6

Access comprehensive regulatory information for “Merit” SPLASHWire Hydrophilic Guide Wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 60663ff73efb62bf8ab5b73d117f30b6 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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60663ff73efb62bf8ab5b73d117f30b6
Registration Details
Taiwan FDA Registration: 60663ff73efb62bf8ab5b73d117f30b6
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Device Details

“Merit” SPLASHWire Hydrophilic Guide Wire
TW: “美瑞特” 史普勒斯親水性導引導線
Risk Class 2
MD

Registration Details

60663ff73efb62bf8ab5b73d117f30b6

Ministry of Health Medical Device Import No. 034514

DHA05603451409

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

Apr 29, 2021

Apr 29, 2026