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“OLYMPUS” VISERA ELITE III VIDEO SYSTEM CENTER - Taiwan Registration 635f27807ed92fdf76ff8c566fd7f27d

Access comprehensive regulatory information for “OLYMPUS” VISERA ELITE III VIDEO SYSTEM CENTER in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 635f27807ed92fdf76ff8c566fd7f27d 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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635f27807ed92fdf76ff8c566fd7f27d
Registration Details
Taiwan FDA Registration: 635f27807ed92fdf76ff8c566fd7f27d
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Device Details

“OLYMPUS” VISERA ELITE III VIDEO SYSTEM CENTER
TW: “奧林柏斯”影像系統主機及附件
Risk Class 2
MD

Registration Details

635f27807ed92fdf76ff8c566fd7f27d

Ministry of Health Medical Device Import No. 036803

DHA05603680300

Company Information

Product Details

Details are as detailed as approved Chinese instructions

H Gastroenterology and urology

H1500 endoscope and accessories

Imported from abroad

Dates and Status

Oct 13, 2023

Oct 13, 2028