Taiwan FDA registration 3db1b23dc073dd07ec228ac50d89f42f
“ROODINSEAT” Rolling Pad (Non-Sterile)
TW: “鑫成”移位滑墊 (未滅菌)
Taiwan·Risk Class 1·MD·ROODINSEAT CORPORATION·Registered Aug 30, 2019 – Aug 30, 2024CancelledRegistration details
- Analysis ID
- 3db1b23dc073dd07ec228ac50d89f42f
- License Form
- Ministry of Health Medical Device Manufacturing No. 007924
Company information
- Manufacturer
- ROODINSEAT CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ROODINSEAT CORPORATION
Product details
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J6785 Manual Patient Conveyor
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Aug 30, 2019
- Expiry Date
- Aug 30, 2024
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for “ROODINSEAT” Rolling Pad (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 3db1b23dc073dd07ec228ac50d89f42f and manufactured by ROODINSEAT CORPORATION. The authorized representative in Taiwan is ROODINSEAT CORPORATION.
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