Taiwan FDA registration c0d14a0db7a56010ef82a71174dfdb66

“OLYMPUS” Single Use Biopsy Forceps

TW: “奧林柏斯”單次使用切片鉗
Taiwan flagTaiwan·Risk Class 2·MD·AOMORI OLYMPUS CO., LTD.·Registered Jul 31, 2021 – Jul 31, 2026Active
Registration details
Analysis ID
c0d14a0db7a56010ef82a71174dfdb66
License Form
Ministry of Health Medical Device Import No. 034799
Customs Code
DHA05603479902
Company information
Manufacturer Country
Japan
Authorized Representative
YUAN LI INSTRUMENT CO., LTD.
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
H Gastroenterology-urology devices
Product Type (Level 2)
H1500 endoscope and accessories
Import Information
Imported from abroad
Dates and status
Registration Date
Jul 31, 2021
Expiry Date
Jul 31, 2026
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About this record

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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