Taiwan FDA registration 3e721d704d5ce2d0330d16752676240f
"Kemai" neuroendoscopic system
TW: “科脈”神經內視鏡系統
Taiwan·Risk Class 2·NEW DEANTRONICS TAIWAN LTD.·Registered Oct 18, 2021 – Oct 18, 2026ActiveRegistration details
- Analysis ID
- 3e721d704d5ce2d0330d16752676240f
Company information
- Manufacturer
- NEW DEANTRONICS TAIWAN LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Clearmind Biomedical Inc.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.4060 腦室套管;; K.1480 神經學科用內視鏡
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Oct 18, 2021
- Expiry Date
- Oct 18, 2026
About this record
Access comprehensive regulatory information for "Kemai" neuroendoscopic system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3e721d704d5ce2d0330d16752676240f and manufactured by NEW DEANTRONICS TAIWAN LTD.. The authorized representative in Taiwan is Clearmind Biomedical Inc..
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