Taiwan FDA registration a6eecea342d2711fee1f314927452801
“Liesien” Cushion (Non-Sterile)
TW: “立薪” 氣墊座(未滅菌)
Taiwan·Risk Class 1·MD·SUPRACOR SYSTEMS, INC.·Registered Sep 01, 2021 – Sep 01, 2026ActiveRegistration details
- Analysis ID
- a6eecea342d2711fee1f314927452801
- License Form
- Ministry of Health Medical Device Import No. 022632
- Customs Code
- DHA09402263206
Company information
- Manufacturer
- SUPRACOR SYSTEMS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- LIESIEN ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the "floating cushion (O.3175)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3175 floating seat cushion
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 01, 2021
- Expiry Date
- Sep 01, 2026
About this record
Access comprehensive regulatory information for “Liesien” Cushion (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a6eecea342d2711fee1f314927452801 and manufactured by SUPRACOR SYSTEMS, INC.. The authorized representative in Taiwan is LIESIEN ENTERPRISE CO., LTD..
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