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"Mai Xin" miniature Fuller blood flow to the reduction chamber device - Taiwan Registration 78088c8bb831c07b2b1933d7dc2b7700

Access comprehensive regulatory information for "Mai Xin" miniature 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 78088c8bb831c07b2b1933d7dc2b7700 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. 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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78088c8bb831c07b2b1933d7dc2b7700
Registration Details
Taiwan FDA Registration: 78088c8bb831c07b2b1933d7dc2b7700
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Device Details

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

Registration Details

78088c8bb831c07b2b1933d7dc2b7700

DHA05603275406

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

Aug 10, 2019

Aug 10, 2029