Taiwan FDA registration 9dbf00b7f10186ffcc969e8d68ccdedf
"Renfei" introduction and drainage catheter (sterilization)
TW: “仁斐”導入及引流導管 (滅菌)
Taiwan·Risk Class 1·RANFAC CORP.·Registered Apr 23, 2010 – Apr 23, 2015CancelledRegistration details
- Analysis ID
- 9dbf00b7f10186ffcc969e8d68ccdedf
- Customs Code
- DHA04400876409
Company information
- Manufacturer
- RANFAC CORP.
- Manufacturer Country
- United States
- Authorized Representative
- MEDLIANCE LTD.
Product details
- Intended Use
- Limited to the scope of Grade 1 identification of "Introduction/Drainage Catheters and Their Accessories (I.4200)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4200 Incoming/Drainage Tubes and Accessories
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Apr 23, 2010
- Expiry Date
- Apr 23, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Renfei" introduction and drainage catheter (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9dbf00b7f10186ffcc969e8d68ccdedf and manufactured by RANFAC CORP.. The authorized representative in Taiwan is MEDLIANCE LTD..
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