Taiwan FDA registration 20834d5333ffc8abd582a0c6d1a856ac

"Mai Xin" Avis intracranial support device

TW: “麥新” 艾維斯顱內支承裝置
Taiwan flagTaiwan·Risk Class 3·MicroVention Europe SARL;; MicroVention Costa Rica·Registered Aug 01, 2023 – Aug 01, 2028Active
Registration details
Analysis ID
20834d5333ffc8abd582a0c6d1a856ac
Customs Code
DHA05603668609
Company information
Manufacturer Country
Costa Rica;;France
Authorized Representative
HOPE SHUN INTERNATIONAL INC.
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
K Neuroscience
Product Type (Level 2)
K.5950 Artificial embolization device
Import Information
import
Dates and status
Registration Date
Aug 01, 2023
Expiry Date
Aug 01, 2028
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About this record

Access comprehensive regulatory information for "Mai Xin" Avis intracranial support device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 20834d5333ffc8abd582a0c6d1a856ac and manufactured by MicroVention Europe SARL;; MicroVention Costa Rica. 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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