Taiwan FDA registration 9f2937d157e5ed19a0616670e598114e
“ROODINSEAT” Cube Gel Cushion(Non-Sterile)
TW: “鑫成” 液態凝膠座墊(未滅菌)
Taiwan·Risk Class 1·MD·ROODINSEAT CORPORATION·Registered Dec 24, 2019 – Dec 24, 2024ExpiredRegistration details
- Analysis ID
- 9f2937d157e5ed19a0616670e598114e
- License Form
- Ministry of Health Medical Device Manufacturing No. 008103
Company information
- Manufacturer
- ROODINSEAT CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ROODINSEAT CORPORATION
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
Dates and status
- Registration Date
- Dec 24, 2019
- Expiry Date
- Dec 24, 2024
About this record
Access comprehensive regulatory information for “ROODINSEAT” Cube Gel 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 9f2937d157e5ed19a0616670e598114e and manufactured by ROODINSEAT CORPORATION. The authorized representative in Taiwan is ROODINSEAT CORPORATION.
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