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“OLYMPUS” Single Use Guide Sheath Kit - Taiwan Registration 913b792d874769ec32dee07fbe3979be

Access comprehensive regulatory information for “OLYMPUS” Single Use Guide Sheath Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 913b792d874769ec32dee07fbe3979be 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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913b792d874769ec32dee07fbe3979be
Registration Details
Taiwan FDA Registration: 913b792d874769ec32dee07fbe3979be
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Device Details

“OLYMPUS” Single Use Guide Sheath Kit
TW: “奧林柏斯”單次使用導引套管組
Risk Class 2
MD

Registration Details

913b792d874769ec32dee07fbe3979be

Ministry of Health Medical Device Import No. 033443

DHA05603344307

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

Apr 19, 2020

Apr 19, 2025