Taiwan FDA registration 6ac07f772114fe3815438590a5448f54

"Maixin" Fuller blood flow to the reduction chamber device

TW: “麥新”孚瑞德血液流向重定腔內裝置
Taiwan flagTaiwan·Risk Class 3·MicroVention Europe SARL; MicroVention, Inc.·Registered Apr 30, 2024 – Apr 30, 2029Active
Registration details
Analysis ID
6ac07f772114fe3815438590a5448f54
Customs Code
DHA05603715700
Company information
Manufacturer Country
France;;United States
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
Apr 30, 2024
Expiry Date
Apr 30, 2029
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About this record

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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