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"Maixin" Fuller blood flow to the reduction chamber device - Taiwan Registration d4e9e2ef490acb9070319a69fd9bbe34

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 d4e9e2ef490acb9070319a69fd9bbe34 and manufactured by MicroVention Europe SARL;; MicroVention Costa Rica S.R.L.. 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, Inc., 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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d4e9e2ef490acb9070319a69fd9bbe34
Registration Details
Taiwan FDA Registration: d4e9e2ef490acb9070319a69fd9bbe34
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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

d4e9e2ef490acb9070319a69fd9bbe34

DHA05603104307

Company Information

Product Details

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

K Neuroscience

K.5950 Artificial embolization device

import

Dates and Status

Apr 20, 2018

Apr 20, 2028

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