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“Teleflex Arrow” Balloon Wedge Pressure Catheters - Taiwan Registration 517f76167d0a09b7726c7e9bcd30883c

Access comprehensive regulatory information for “Teleflex Arrow” Balloon Wedge Pressure Catheters in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 517f76167d0a09b7726c7e9bcd30883c and manufactured by Arrow International, LLC (Subsidiary of Teleflex, Incorporated). The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..

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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517f76167d0a09b7726c7e9bcd30883c
Registration Details
Taiwan FDA Registration: 517f76167d0a09b7726c7e9bcd30883c
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Device Details

“Teleflex Arrow” Balloon Wedge Pressure Catheters
TW: “泰利福亞諾”肺動脈氣壓導管
Risk Class 2
MD

Registration Details

517f76167d0a09b7726c7e9bcd30883c

Ministry of Health Medical Device Import No. 030911

DHA05603091102

Company Information

Product Details

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

E Cardiovascular devices

E1240 flow guide duct

Imported from abroad

Dates and Status

May 31, 2018

May 31, 2023