Taiwan FDA registration 497670d646f8b0d324d2db46bf291100
“Acandis” Derivo Embolisation Device
TW: “艾康蒂”德瑞佛栓塞裝置
Taiwan·Risk Class 3·MD·Acandis GmbH·Registered Jul 27, 2018 – Jul 27, 2028ActiveRegistration details
- Analysis ID
- 497670d646f8b0d324d2db46bf291100
- License Form
- Ministry of Health Medical Device Import No. 031373
- Customs Code
- DHA05603137302
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)
- K Devices for neuroscience
- Product Type (Level 2)
- K5950 Artificial embolization device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 27, 2018
- Expiry Date
- Jul 27, 2028
About this record
Access comprehensive regulatory information for “Acandis” Derivo Embolisation Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 497670d646f8b0d324d2db46bf291100 and manufactured by Acandis GmbH. The authorized representative in Taiwan is DR SHAO MD REGULATORY CONSULTANTS CO., LTD..
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