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“OLYMPUS” Single Use Aspiration Needle - Taiwan Registration ce778d65848f70d48112f71e5fe5cae8

Access comprehensive regulatory information for “OLYMPUS” Single Use Aspiration Needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ce778d65848f70d48112f71e5fe5cae8 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, 2 companies making similar products including AOMORI OLYMPUS CO., LTD., Gyrus ACMI, Inc., and 4 recent registrations in the same category. 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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ce778d65848f70d48112f71e5fe5cae8
Registration Details
Taiwan FDA Registration: ce778d65848f70d48112f71e5fe5cae8
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Device Details

“OLYMPUS” Single Use Aspiration Needle
TW: “奧林柏斯”單次使用抽吸生檢針
Risk Class 2
MD

Registration Details

ce778d65848f70d48112f71e5fe5cae8

Ministry of Health Medical Device Import No. 029017

DHA05602901701

Company Information

Japan

Product Details

For details, it is Chinese approved copy of the imitation order

H Gastroenterology-urology devices

H1075 Gastroenterology - Urology biopsy instruments

Imported from abroad

Dates and Status

Nov 07, 2016

Nov 07, 2026

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