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“OLYMPUS” Visera Elite II Xenon Light Source - Taiwan Registration 9fe9368b4786eb0810b5f687d2d7246c

Access comprehensive regulatory information for “OLYMPUS” Visera Elite II Xenon Light Source in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9fe9368b4786eb0810b5f687d2d7246c and manufactured by SHIRAKAWA 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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9fe9368b4786eb0810b5f687d2d7246c
Registration Details
Taiwan FDA Registration: 9fe9368b4786eb0810b5f687d2d7246c
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Device Details

“OLYMPUS” Visera Elite II Xenon Light Source
TW: “奧林柏斯”內視鏡用光源裝置及附件
Risk Class 2
MD

Registration Details

9fe9368b4786eb0810b5f687d2d7246c

Ministry of Health Medical Device Import No. 031009

DHA05603100907

Company Information

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

Mar 30, 2018

Mar 30, 2028