Taiwan FDA registration 11b8a5ae226a2494f2c1b9abf7342618

“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 Sep 04, 2018 – Sep 04, 2028Active
Registration details
Analysis ID
11b8a5ae226a2494f2c1b9abf7342618
License Form
Ministry of Health Medical Device Import No. 031589
Customs Code
DHA05603158902
Company information
Manufacturer Country
Japan
Authorized Representative
YUAN LI INSTRUMENT CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
H Gastroenterology-urology devices
Product Type (Level 2)
H1075 Gastroenterology - Urology biopsy instruments
Import Information
Imported from abroad
Dates and status
Registration Date
Sep 04, 2018
Expiry Date
Sep 04, 2028
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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 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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