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“OLYMPUS” SINGLE USE SPLINTING TUBE - Taiwan Registration 34b0c9dbcaaf1ce3473d41e9457d0338

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 34b0c9dbcaaf1ce3473d41e9457d0338 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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34b0c9dbcaaf1ce3473d41e9457d0338
Registration Details
Taiwan FDA Registration: 34b0c9dbcaaf1ce3473d41e9457d0338
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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

34b0c9dbcaaf1ce3473d41e9457d0338

Ministry of Health Medical Device Import No. 029648

DHA05602964800

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

Apr 25, 2017

Apr 25, 2027

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