Taiwan FDA registration e04cd8d223fe87a558854a8bb5d28da7
"Recher" foreign object gripper
TW: “睿取爾”異物夾取器
Taiwan·Risk Class 2·RADIUS MEDICAL TECHNOLOGIES, INC.·Registered Aug 11, 2009 – Aug 11, 2014CancelledRegistration details
- Analysis ID
- e04cd8d223fe87a558854a8bb5d28da7
- Customs Code
- DHA00602010703
Company information
- Manufacturer
- RADIUS MEDICAL TECHNOLOGIES, INC.
- Manufacturer Country
- United States
- Authorized Representative
- WATTCAN INSTRUMENTS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- Aug 11, 2009
- Expiry Date
- Aug 11, 2014
- Cancellation Date
- Jun 26, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Recher" foreign object gripper in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e04cd8d223fe87a558854a8bb5d28da7 and manufactured by RADIUS MEDICAL TECHNOLOGIES, INC.. The authorized representative in Taiwan is WATTCAN INSTRUMENTS CO., LTD..
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