Taiwan FDA registration 9f2bdf283b0cb4ab4091baf18cce60ab
"Jianpeng" gel seat cushion (unsterilized)
TW: "建鵬" 凝膠座墊 (未滅菌)
Taiwan·Risk Class 1·ROODINSEAT CORPORATION·Registered Oct 08, 2019 – Oct 08, 2029ActiveRegistration details
- Analysis ID
- 9f2bdf283b0cb4ab4091baf18cce60ab
Company information
- Manufacturer
- ROODINSEAT CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- J. P. CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the "floating cushion (O.3175)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3175 Floating cushion
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Oct 08, 2019
- Expiry Date
- Oct 08, 2029
About this record
Access comprehensive regulatory information for "Jianpeng" gel seat cushion (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9f2bdf283b0cb4ab4091baf18cce60ab and manufactured by ROODINSEAT CORPORATION. The authorized representative in Taiwan is J. P. CO., LTD..
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