Pure Global

“OLYMPUS” SINGLE USE SPLINTING TUBE - Taiwan Registration a0e766ceecfc9a57fece71cb55c76950

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
1 Competitors
1 Recent Registrations
a0e766ceecfc9a57fece71cb55c76950
Registration Details
Taiwan FDA Registration: a0e766ceecfc9a57fece71cb55c76950
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“OLYMPUS” SINGLE USE SPLINTING TUBE
TW: “奧林柏斯”單次使用固定管
Risk Class 2
MD

Registration Details

a0e766ceecfc9a57fece71cb55c76950

Ministry of Health Medical Device Import No. 029862

DHA05602986202

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

H Gastroenterology-urology devices

H1500 endoscope and accessories

Imported from abroad

Dates and Status

May 25, 2017

May 25, 2027

Companies Making Similar Products
Top companies providing products similar to "“OLYMPUS” SINGLE USE SPLINTING TUBE"