Pure Global

“OLYMPUS” EVIS LUCERA ELITE DUODENOVIDEOSCOPE - Taiwan Registration 6084e5802f51ee48a2d6d7c56c561594

Access comprehensive regulatory information for “OLYMPUS” EVIS LUCERA ELITE DUODENOVIDEOSCOPE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6084e5802f51ee48a2d6d7c56c561594 and manufactured by AIZU 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
6084e5802f51ee48a2d6d7c56c561594
Registration Details
Taiwan FDA Registration: 6084e5802f51ee48a2d6d7c56c561594
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“OLYMPUS” EVIS LUCERA ELITE DUODENOVIDEOSCOPE
TW: “奧林柏斯”處置型十二指腸鏡
Risk Class 2
MD

Registration Details

6084e5802f51ee48a2d6d7c56c561594

Ministry of Health Medical Device Import No. 034989

DHA05603498904

Company Information

Japan

Product Details

Details are as detailed as approved Chinese instructions

H Gastroenterology-urology devices

H1500 endoscope and accessories

Imported from abroad

Dates and Status

Oct 28, 2021

Oct 28, 2026