Taiwan FDA registration dd4595987976de21ce610d13d8104697
“Huasyn” Flotation Cushion (Non-Sterile)
TW: “華莘”浮動坐墊(未滅菌)
Taiwan·Risk Class 1·MD·RECFRANCE·Registered Mar 02, 2022 – Mar 02, 2027ActiveRegistration details
- Analysis ID
- dd4595987976de21ce610d13d8104697
- License Form
- Ministry of Health Medical Device Import No. 022752
- Customs Code
- DHA09402275203
Company information
- Manufacturer
- RECFRANCE
- Manufacturer Country
- France
- Authorized Representative
- HUASYN BIOMEDICAL 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 Physical Medical Sciences
- Product Type (Level 2)
- O3175 floating seat cushion
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 02, 2022
- Expiry Date
- Mar 02, 2027
About this record
Access comprehensive regulatory information for “Huasyn” 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 dd4595987976de21ce610d13d8104697 and manufactured by RECFRANCE. The authorized representative in Taiwan is HUASYN BIOMEDICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices