Taiwan FDA registration eb247ea1f23bf6485ab1116fe3da9673

“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 Feb 21, 2019 – Feb 21, 2029Active
Registration details
Analysis ID
eb247ea1f23bf6485ab1116fe3da9673
License Form
Ministry of Health Medical Device Import No. 032257
Customs Code
DHA05603225705
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)
H1500 endoscope and accessories
Import Information
Imported from abroad
Dates and status
Registration Date
Feb 21, 2019
Expiry Date
Feb 21, 2029
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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 eb247ea1f23bf6485ab1116fe3da9673 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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