Taiwan FDA registration fe0da88027ce23f336c6631aabcdf17c
"Angelaid" Nonpowered flotation therapy mattress (Non-Sterile)
TW: "天使愛" 非動力式治療床墊 (未滅菌)
Taiwan·Risk Class 1·MD·Hongdayi Enterprise Co., Ltd. Medical Materials Factory·Registered Apr 19, 2019 – Apr 19, 2024CancelledRegistration details
- Analysis ID
- fe0da88027ce23f336c6631aabcdf17c
- License Form
- Ministry of Health Medical Device Manufacturing No. 007728
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- WELL LANDS ENTERPRISE CO., LTD.
Product details
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5150 Non-powered treatment mattress
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Apr 19, 2019
- Expiry Date
- Apr 19, 2024
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "Angelaid" Nonpowered flotation therapy mattress (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 fe0da88027ce23f336c6631aabcdf17c and manufactured by Hongdayi Enterprise Co., Ltd. Medical Materials Factory. The authorized representative in Taiwan is WELL LANDS ENTERPRISE 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