Taiwan FDA registration 50f33b9bea509b325b2ab61197023b07
“Invacare” Flo-tech Solution Xtra Flotation Cushion (Non-Sterile)
TW: “英維康” 凝膠減壓座墊(未滅菌)
Taiwan·Risk Class 1·MD·Invacare UK - Operations Ltd·Registered Sep 13, 2021 – Sep 13, 2026ActiveRegistration details
- Analysis ID
- 50f33b9bea509b325b2ab61197023b07
- License Form
- Ministry of Health Medical Device Import No. 022648
- Customs Code
- DHA09402264808
Company information
- Manufacturer
- Invacare UK - Operations Ltd
- Manufacturer Country
- United Kingdom
- Authorized Representative
- Wellell Inc.
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 13, 2021
- Expiry Date
- Sep 13, 2026
About this record
Access comprehensive regulatory information for “Invacare” Flo-tech Solution Xtra Flotation 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 50f33b9bea509b325b2ab61197023b07 and manufactured by Invacare UK - Operations Ltd. The authorized representative in Taiwan is Wellell Inc..
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