Taiwan FDA registration 13d3216eb63071c2abe9dbc7ad8e9736
"Qinda" belly pad (sterile/unsterilized)
TW: "勤達" 腹部墊 (滅菌/未滅菌)
Taiwan·Risk Class 1·HOSPITECH MANUFACTURING SERVICES SDN BHD·Registered Jun 29, 2012 – Jun 29, 2022CancelledRegistration details
- Analysis ID
- 13d3216eb63071c2abe9dbc7ad8e9736
- Customs Code
- DHA04401189801
Company information
- Manufacturer
- HOSPITECH MANUFACTURING SERVICES SDN BHD
- Manufacturer Country
- Malaysia
- Authorized Representative
- TEAM POWER MEDICAL INSTRUMENT LTD.
Product details
- Intended Use
- Limited to the first level of identification range of "unabsorbed gauze for in vivo (I.4450)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4450 Non-absorbable filament cloth for internal use
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Jun 29, 2012
- Expiry Date
- Jun 29, 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 "Qinda" belly pad (sterile/unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 13d3216eb63071c2abe9dbc7ad8e9736 and manufactured by HOSPITECH MANUFACTURING SERVICES SDN BHD. The authorized representative in Taiwan is TEAM POWER MEDICAL INSTRUMENT LTD..
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