Taiwan FDA registration 389660fda20bf6aadca5aa58ae79ff5f
"Miraco" Flotation cushion (Non-Sterile)
TW: "美樂克" 減壓坐墊 (未滅菌)
Registration details
- Analysis ID
- 389660fda20bf6aadca5aa58ae79ff5f
- License Form
- Ministry of Health Medical Device Manufacturing No. 007864
Company information
- Manufacturer
- SIFO Healthcare Corporation
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HORIZON INSTRUMENTS CO. ,LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Floating Cushion (O.3175)".
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3175 floating seat cushion
- Import Information
- Produced in Taiwan, China; Contract manufacturing
Dates and status
- Registration Date
- Jul 19, 2019
- Expiry Date
- Jul 19, 2024
About this record
Access comprehensive regulatory information for "Miraco" 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 389660fda20bf6aadca5aa58ae79ff5f and manufactured by SIFO Healthcare Corporation. The authorized representative in Taiwan is HORIZON INSTRUMENTS CO. ,LTD..
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