Taiwan FDA registration 18344d3737be3268e9f1201dd661dd0b
"Qinda" non-respiratory medical sprayer (unsterilized)
TW: “勤達”非呼吸用醫藥噴霧器(未滅菌)
Taiwan·Risk Class 1·HOSPITECH MANUFACTURING SERVICES SDN BHD·Registered Apr 16, 2012 – Apr 16, 2022CancelledRegistration details
- Analysis ID
- 18344d3737be3268e9f1201dd661dd0b
- Customs Code
- DHA04401160206
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 "Non-respiratory Medical Aerosol Device (D.5640)".
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5640 非呼吸用醫藥噴霧器(atomizer)
- Import Information
- import
Dates and status
- Registration Date
- Apr 16, 2012
- Expiry Date
- Apr 16, 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" non-respiratory medical sprayer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 18344d3737be3268e9f1201dd661dd0b and manufactured by HOSPITECH MANUFACTURING SERVICES SDN BHD. The authorized representative in Taiwan is TEAM POWER MEDICAL INSTRUMENT LTD..
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