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“Gyrus ACMI” E-Z Grip Guidewire Torque Device - Taiwan Registration 461a07517a167048632b13e5b950552e

Access comprehensive regulatory information for “Gyrus ACMI” E-Z Grip Guidewire Torque Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 461a07517a167048632b13e5b950552e and manufactured by Gyrus ACMI, Inc.. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., 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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461a07517a167048632b13e5b950552e
Registration Details
Taiwan FDA Registration: 461a07517a167048632b13e5b950552e
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Device Details

“Gyrus ACMI” E-Z Grip Guidewire Torque Device
TW: “吉洛氏 艾斯米”簡易導引線扭矩裝置
Risk Class 2
MD

Registration Details

461a07517a167048632b13e5b950552e

Ministry of Health Medical Device Import No. 026876

DHA05602687608

Company Information

United States

Product Details

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

H Gastroenterology-urology devices

H1500 endoscope and accessories

Imported from abroad

Dates and Status

Dec 25, 2014

Dec 25, 2024