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“Quest” Artemis Handheld System - Taiwan Registration 3b4a1897a7558344fd9204e0b565c56a

Access comprehensive regulatory information for “Quest” Artemis Handheld System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3b4a1897a7558344fd9204e0b565c56a and manufactured by Quest Medical Imaging. The authorized representative in Taiwan is Yuanyou Industrial 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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3b4a1897a7558344fd9204e0b565c56a
Registration Details
Taiwan FDA Registration: 3b4a1897a7558344fd9204e0b565c56a
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Device Details

“Quest” Artemis Handheld System
TW: “奎斯特”阿蒂蜜絲手術用內視鏡系統
Risk Class 2
MD

Registration Details

3b4a1897a7558344fd9204e0b565c56a

Ministry of Health Medical Device Import No. 029391

DHA05602939102

Company Information

Netherlands

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

Feb 17, 2017

Feb 17, 2022