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"Porter" cap revascularization device - Taiwan Registration 9e8794bb2be24aeee6c2ac92f577f7fa

Access comprehensive regulatory information for "Porter" cap revascularization device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9e8794bb2be24aeee6c2ac92f577f7fa and manufactured by BALT EXTRUSION SAS. The authorized representative in Taiwan is EVERMED MEDICAL ENTERPRISE CO., LTD..

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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9e8794bb2be24aeee6c2ac92f577f7fa
Registration Details
Taiwan FDA Registration: 9e8794bb2be24aeee6c2ac92f577f7fa
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Device Details

"Porter" cap revascularization device
TW: โ€œๆณข็‰นโ€่“‹ๅ–่ก€็ฎก้‡ๅปบ่ฃ็ฝฎ
Risk Class 2

Registration Details

9e8794bb2be24aeee6c2ac92f577f7fa

DHA05603766506

Company Information

France

Product Details

Details are as detailed as approved Chinese instructions

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K.5600 Neurovascular mechanical clot removal device for the treatment of acute ischemic stroke

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Dates and Status

Nov 27, 2024

Nov 27, 2029