Taiwan FDA registration 5e3c8e44a3eeeca7fcae6dd0b5f62641
"Cloudcatch" non-aerated hemostatic device (unsterilized)
TW: "云采" 非充氣式止血器 (未滅菌)
Taiwan·Risk Class 1·TAHAN BIOMEDICAL CO., LTD.·Registered Oct 02, 2017 – Oct 02, 2022CancelledRegistration details
- Analysis ID
- 5e3c8e44a3eeeca7fcae6dd0b5f62641
Company information
- Manufacturer
- TAHAN BIOMEDICAL CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Yuncai Biotechnology Co., Ltd
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Non-inflatable Tourniquet (I.5900)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.5900 非充氣式止血帶
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Oct 02, 2017
- Expiry Date
- Oct 02, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Cloudcatch" non-aerated hemostatic device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5e3c8e44a3eeeca7fcae6dd0b5f62641 and manufactured by TAHAN BIOMEDICAL CO., LTD.. The authorized representative in Taiwan is Yuncai Biotechnology Co., Ltd.
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