Taiwan FDA registration ce778d65848f70d48112f71e5fe5cae8

“OLYMPUS” Single Use Aspiration Needle

TW: “奧林柏斯”單次使用抽吸生檢針
Taiwan flagTaiwan·Risk Class 2·MD·AOMORI OLYMPUS CO., LTD.·Registered Nov 07, 2016 – Nov 07, 2026Active
Registration details
Analysis ID
ce778d65848f70d48112f71e5fe5cae8
License Form
Ministry of Health Medical Device Import No. 029017
Customs Code
DHA05602901701
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
Nov 07, 2016
Expiry Date
Nov 07, 2026
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About this record

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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