Taiwan FDA registration 2161b4113e32133b493585d3d74c287c
"EMANA" Limb orthosis (Non-Sterile)
TW: "日滕" 肢體裝具 (未滅菌)
Taiwan·Risk Class 1·MD·SHENGDEI TECHNOLOGY CO., LTD.·Registered Sep 19, 2019 – Sep 19, 2024CancelledRegistration details
- Analysis ID
- 2161b4113e32133b493585d3d74c287c
- License Form
- Ministry of Health Medical Device Manufacturing No. 007959
Company information
- Manufacturer
- SHENGDEI TECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Riteng Biomedical Co., Ltd
Product details
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3475 Body Equipment
- Import Information
- Produced in Taiwan, China; Contract manufacturing
Dates and status
- Registration Date
- Sep 19, 2019
- Expiry Date
- Sep 19, 2024
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "EMANA" Limb orthosis (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 2161b4113e32133b493585d3d74c287c and manufactured by SHENGDEI TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is Riteng Biomedical Co., Ltd.
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