Taiwan FDA registration 2d70e0c768a86f1424c8cf91e2721bf0
"Yuefa" gel seat cushion (unsterilized)
TW: "悅發" 凝膠座墊 (未滅菌)
Registration details
- Analysis ID
- 2d70e0c768a86f1424c8cf91e2721bf0
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PE & LE ENTERPRISE 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)
- O.3175 Floating cushion
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Jun 06, 2019
- Expiry Date
- Jun 06, 2029
About this record
Access comprehensive regulatory information for "Yuefa" gel seat cushion (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2d70e0c768a86f1424c8cf91e2721bf0 and manufactured by Paili Enterprises Limited;; Hongdayi Enterprise Co., Ltd. Medical Material Factory. The authorized representative in Taiwan is PE & LE ENTERPRISE 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