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“OLYMPUS” Single Use Biopsy Forceps - Taiwan Registration c0d14a0db7a56010ef82a71174dfdb66

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 c0d14a0db7a56010ef82a71174dfdb66 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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c0d14a0db7a56010ef82a71174dfdb66
Registration Details
Taiwan FDA Registration: c0d14a0db7a56010ef82a71174dfdb66
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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

c0d14a0db7a56010ef82a71174dfdb66

Ministry of Health Medical Device Import No. 034799

DHA05603479902

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

Jul 31, 2021

Jul 31, 2026

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