Taiwan FDA registration 78088c8bb831c07b2b1933d7dc2b7700
"Mai Xin" miniature Fuller blood flow to the reduction chamber device
TW: “麥新”微型孚瑞德血液流向重定腔內裝置
Taiwan·Risk Class 3·MicroVention Europe SARL;; MicroVention Costa Rica S.R.L.·Registered Aug 10, 2019 – Aug 10, 2029ActiveRegistration details
- Analysis ID
- 78088c8bb831c07b2b1933d7dc2b7700
- Customs Code
- DHA05603275406
Company information
- Manufacturer Country
- Costa Rica;;France
- Authorized Representative
- HOPE SHUN INTERNATIONAL INC.
Product details
- 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
Dates and status
- Registration Date
- Aug 10, 2019
- Expiry Date
- Aug 10, 2029
About this record
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..
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