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"Okutai" plugging propeller - Taiwan Registration 9742a17fc0d8486c20f660bc604a478e

Access comprehensive regulatory information for "Okutai" plugging propeller in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9742a17fc0d8486c20f660bc604a478e and manufactured by Occlutech GmbH. The authorized representative in Taiwan is MEDICARE UNITECH INC..

This page provides complete technical specifications, regulatory compliance details. 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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9742a17fc0d8486c20f660bc604a478e
Registration Details
Taiwan FDA Registration: 9742a17fc0d8486c20f660bc604a478e
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Device Details

"Okutai" plugging propeller
TW: โ€œๅฅงๅบซๆณฐโ€ๅฐๅ ตๅ™จๆŽจ้€ฒๅ™จ
Risk Class 2

Registration Details

9742a17fc0d8486c20f660bc604a478e

DHA05603605704

Company Information

Germany

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Nov 25, 2022

Nov 25, 2027