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“OLYMPUS” Single Use Guiding Device - Taiwan Registration 9d88c17c62dfc5292855a019515391ef

Access comprehensive regulatory information for “OLYMPUS” Single Use Guiding Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9d88c17c62dfc5292855a019515391ef and manufactured by AOMORI OLYMPUS CO., LTD.. 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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9d88c17c62dfc5292855a019515391ef
Registration Details
Taiwan FDA Registration: 9d88c17c62dfc5292855a019515391ef
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Device Details

“OLYMPUS” Single Use Guiding Device
TW: “奧林柏斯”單次使用導引裝置
Risk Class 2
MD

Registration Details

9d88c17c62dfc5292855a019515391ef

Ministry of Health Medical Device Import No. 030038

DHA05603003809

Company Information

Japan

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

Jul 31, 2017

Jul 31, 2027