Taiwan FDA registration 214ed94fbd7d84ca02647bb692c4229f
"Qinda" liquid drug dispenser (unsterilized)
TW: “勤達”液體藥物給藥器 (未滅菌)
Taiwan·Risk Class 1·HOSPITECH MANUFACTURING SERVICES SDN. BHD.·Registered Jun 06, 2008 – Jun 06, 2023ExpiredRegistration details
- Analysis ID
- 214ed94fbd7d84ca02647bb692c4229f
- Customs Code
- DHA04400679408
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 scope of the Measures for the Administration of Medical Devices "Liquid Drug Dispenser (J.6430)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6430 液體藥物給藥器
- Import Information
- import
Dates and status
- Registration Date
- Jun 06, 2008
- Expiry Date
- Jun 06, 2023
About this record
Access comprehensive regulatory information for "Qinda" liquid drug dispenser (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 214ed94fbd7d84ca02647bb692c4229f and manufactured by HOSPITECH MANUFACTURING SERVICES SDN. BHD.. The authorized representative in Taiwan is TEAM POWER MEDICAL INSTRUMENT LTD..
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