"Maixin" Fuller blood flow to the reduction chamber device
Taiwan·Risk Class 3·MicroVention Europe SARL;; MicroVention Costa Rica S.R.L.·Registered Apr 20, 2018 – Apr 20, 2028Active- Analysis ID
- d4e9e2ef490acb9070319a69fd9bbe34
- Customs Code
- DHA05603104307
- Manufacturer Country
- Costa Rica;;France
- Authorized Representative
- HOPE SHUN INTERNATIONAL INC.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.5950 Artificial embolization device
- Import Information
- import
- Registration Date
- Apr 20, 2018
- Expiry Date
- Apr 20, 2028
Top companies providing products similar to ""Maixin" Fuller blood flow to the reduction chamber device"
Recently registered similar products
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.