Taiwan FDA registration bf44b4d54d8281b438392df85b02b0b0
“B. Braun” Aesculap MINOP InVent Intraventricular Neuroendoscopy
TW: “柏朗”雅氏腦室內視鏡
Taiwan·Risk Class 2·MD·AESCULAP AG·Registered Dec 10, 2018 – Dec 10, 2028ActiveRegistration details
- Analysis ID
- bf44b4d54d8281b438392df85b02b0b0
- License Form
- Ministry of Health Medical Device Import No. 031920
- Customs Code
- DHA05603192005
Company information
- Manufacturer
- AESCULAP AG
- Manufacturer Country
- Germany
- Authorized Representative
- B. BRAUN TAIWAN CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Devices for neuroscience
- Product Type (Level 2)
- K1480 Endoscope for neuroscience
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 10, 2018
- Expiry Date
- Dec 10, 2028
About this record
Access comprehensive regulatory information for “B. Braun” Aesculap MINOP InVent Intraventricular Neuroendoscopy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bf44b4d54d8281b438392df85b02b0b0 and manufactured by AESCULAP AG. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..
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