Taiwan FDA registration a0e766ceecfc9a57fece71cb55c76950

“OLYMPUS” SINGLE USE SPLINTING TUBE

TW: “奧林柏斯”單次使用固定管
Taiwan flagTaiwan·Risk Class 2·MD·Olympus Medical Systems Corp. Hinode Plant·Registered May 25, 2017 – May 25, 2027Active
Registration details
Analysis ID
a0e766ceecfc9a57fece71cb55c76950
License Form
Ministry of Health Medical Device Import No. 029862
Customs Code
DHA05602986202
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
May 25, 2017
Expiry Date
May 25, 2027
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About this record

Access comprehensive regulatory information for “OLYMPUS” SINGLE USE SPLINTING TUBE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a0e766ceecfc9a57fece71cb55c76950 and manufactured by Olympus Medical Systems Corp. Hinode Plant. 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 Olympus Medical Systems Corp. Hinode Plant, 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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