Taiwan FDA registration eaf0fb2c774496382fd422d14ff5b745
"Qinda" artificial nose (sterilized)
TW: “勤達”人工鼻(滅菌)
Taiwan·Risk Class 1·HOSPITECH MANUFACTURING SERVICES SDN. BHD.·Registered Dec 11, 2007 – Dec 11, 2017CancelledRegistration details
- Analysis ID
- eaf0fb2c774496382fd422d14ff5b745
- Customs Code
- DHA04400637705
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 recognition range of the Measures for the Administration of Medical Devices "Heat and Moisture Condenser (Artificial Nose) (D.5375)".
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5375 Heat and humidity condenser (artificial nose)
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Dec 11, 2007
- Expiry Date
- Dec 11, 2017
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Qinda" artificial nose (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number eaf0fb2c774496382fd422d14ff5b745 and manufactured by HOSPITECH MANUFACTURING SERVICES SDN. BHD.. The authorized representative in Taiwan is TEAM POWER MEDICAL INSTRUMENT LTD..
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