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“OLYMPUS” Single Use Biopsy Forceps - Taiwan Registration 11b8a5ae226a2494f2c1b9abf7342618

Access comprehensive regulatory information for “OLYMPUS” Single Use Biopsy Forceps in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 11b8a5ae226a2494f2c1b9abf7342618 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, 1 companies making similar products including AOMORI OLYMPUS CO., LTD., and 1 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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11b8a5ae226a2494f2c1b9abf7342618
Registration Details
Taiwan FDA Registration: 11b8a5ae226a2494f2c1b9abf7342618
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Device Details

“OLYMPUS” Single Use Biopsy Forceps
TW: “奧林柏斯”單次使用切片鉗
Risk Class 2
MD

Registration Details

11b8a5ae226a2494f2c1b9abf7342618

Ministry of Health Medical Device Import No. 031589

DHA05603158902

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

Sep 04, 2018

Sep 04, 2028

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