Taiwan FDA registration 51c17d9bfb4b775c29bbca169b7951d3
“Camntech” Actiwave System
TW: “坎迪克”生理波形記錄系統
Taiwan·Risk Class 2·MD·CamNtech Ltd·Registered Jan 08, 2016 – Jan 08, 2021CancelledRegistration details
- Analysis ID
- 51c17d9bfb4b775c29bbca169b7951d3
- License Form
- Ministry of Health Medical Device Import No. 028138
- Customs Code
- DHA05602813808
Company information
- Manufacturer
- CamNtech Ltd
- Manufacturer Country
- United Kingdom
- Authorized Representative
- AMY GRANT LTD.
Product details
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E2800 Medical Tape Recorder
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 08, 2016
- Expiry Date
- Jan 08, 2021
- Cancellation Date
- Aug 28, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “Camntech” Actiwave System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 51c17d9bfb4b775c29bbca169b7951d3 and manufactured by CamNtech Ltd. The authorized representative in Taiwan is AMY GRANT LTD..
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