Taiwan FDA registration f29c9555e6b9f4dc6aaa49e0dc338f3d
“Acandis” NeuroBridge Catheter
TW: “艾康蒂”諾布導管
Taiwan·Risk Class 2·MD·Acandis GmbH·Registered Dec 15, 2017 – Dec 15, 2027ActiveRegistration details
- Analysis ID
- f29c9555e6b9f4dc6aaa49e0dc338f3d
- License Form
- Ministry of Health Medical Device Import No. 030618
- Customs Code
- DHA05603061801
Company information
- Manufacturer
- Acandis GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- DR SHAO MD REGULATORY CONSULTANTS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1250 Percutaneous catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 15, 2017
- Expiry Date
- Dec 15, 2027
About this record
Access comprehensive regulatory information for “Acandis” NeuroBridge Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f29c9555e6b9f4dc6aaa49e0dc338f3d and manufactured by Acandis GmbH. The authorized representative in Taiwan is DR SHAO MD REGULATORY CONSULTANTS CO., LTD..
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