Taiwan FDA registration 001f1fac1c31d3a2948c757b1473087f
"Shunlixi" household treatment humidifier (unsterilized)
TW: "順力西" 家用治療潮濕器 (未滅菌)
Taiwan·Risk Class 1·SLS MEDICAL TECHNOLOGY CORP. LTD.·Registered Apr 10, 2013 – Apr 10, 2018CancelledRegistration details
- Analysis ID
- 001f1fac1c31d3a2948c757b1473087f
Company information
- Manufacturer
- SLS MEDICAL TECHNOLOGY CORP. LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SLS MEDICAL TECHNOLOGY CORP. LTD.
Product details
- Intended Use
- Limited to the first level of identification range of the Measures for the Administration of Medical Devices "Household Treatment Moisturizer (D.5460)".
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5460 家用治療潮濕器
- Import Information
- Domestic
Dates and status
- Registration Date
- Apr 10, 2013
- Expiry Date
- Apr 10, 2018
- Cancellation Date
- Oct 25, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Shunlixi" household treatment humidifier (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 001f1fac1c31d3a2948c757b1473087f and manufactured by SLS MEDICAL TECHNOLOGY CORP. LTD.. The authorized representative in Taiwan is SLS MEDICAL TECHNOLOGY CORP. LTD..
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