Taiwan FDA registration 236df9b2dbd9bce9e940d79b305a95c7
"Qinda" medical gauze (sterilization)
TW: “勤達”醫療用紗布(滅菌)
Taiwan·Risk Class 1·HOSPITECH MANUFACTURING SERVICES SDN. BHD.·Registered Sep 20, 2007 – Sep 20, 2022CancelledRegistration details
- Analysis ID
- 236df9b2dbd9bce9e940d79b305a95c7
- Customs Code
- DHA04400616200
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 identification range of the Measures for the Administration of Medical Devices "Medical Absorbent Fiber (J.5300)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5300 醫療用吸收纖維
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Sep 20, 2007
- Expiry Date
- Sep 20, 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" medical gauze (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 236df9b2dbd9bce9e940d79b305a95c7 and manufactured by HOSPITECH MANUFACTURING SERVICES SDN. BHD.. The authorized representative in Taiwan is TEAM POWER MEDICAL INSTRUMENT LTD..
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