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"Maixin" Fuller blood flow to the reduction chamber device - Taiwan Registration 6ac07f772114fe3815438590a5448f54

Access comprehensive regulatory information for "Maixin" Fuller blood flow to the reduction chamber device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 6ac07f772114fe3815438590a5448f54 and manufactured by MicroVention Europe SARL; MicroVention, Inc.. The authorized representative in Taiwan is HOPE SHUN INTERNATIONAL INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MicroVention Europe SARL;; MicroVention Costa Rica S.R.L., 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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6ac07f772114fe3815438590a5448f54
Registration Details
Taiwan FDA Registration: 6ac07f772114fe3815438590a5448f54
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Device Details

"Maixin" Fuller blood flow to the reduction chamber device
TW: โ€œ้บฅๆ–ฐโ€ๅญš็‘žๅพท่ก€ๆถฒๆตๅ‘้‡ๅฎš่…”ๅ…ง่ฃ็ฝฎ
Risk Class 3

Registration Details

6ac07f772114fe3815438590a5448f54

DHA05603715700

Company Information

France;;United States

Product Details

Details are as detailed as approved Chinese instructions

K Neuroscience

K.5950 Artificial embolization device

import

Dates and Status

Apr 30, 2024

Apr 30, 2029

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