"Maixin" Fuller blood flow to the reduction chamber device
- Analysis ID
- 6ac07f772114fe3815438590a5448f54
- Customs Code
- DHA05603715700
- Manufacturer
- MicroVention Europe SARL; MicroVention, Inc.
- Manufacturer Country
- France;;United States
- Authorized Representative
- HOPE SHUN INTERNATIONAL INC.
- 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
- Registration Date
- Apr 30, 2024
- Expiry Date
- Apr 30, 2029
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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.