Taiwan FDA registration fdd9fa01a0e7d2cc81ec3eb3ea74aafb
"Qinda" suction tube (sterilized)
TW: “勤達”抽痰管（滅菌）
Taiwan·Risk Class 1·HOSPITECH MANUFACTURING SERVICES SDN. BHD.·Registered Apr 20, 2007 – Apr 20, 2022CancelledRegistration details
- Analysis ID
- fdd9fa01a0e7d2cc81ec3eb3ea74aafb
- Customs Code
- DHA04400578005
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 management method of medical equipment, tracheobronchial suction catheter (D.6810) level 1 identification range.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.6810 Pneumatic bronchial suction guide tube
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Apr 20, 2007
- Expiry Date
- Apr 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" suction tube (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fdd9fa01a0e7d2cc81ec3eb3ea74aafb and manufactured by HOSPITECH MANUFACTURING SERVICES SDN. BHD.. The authorized representative in Taiwan is TEAM POWER MEDICAL INSTRUMENT LTD..
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