Taiwan FDA registration 883cfa84a0757a71492e7d7c583f9bfe
“Joson Care”Plinth (Non-Sterile)
TW: “強盛興”治療檯(未滅菌)
Taiwan·Risk Class 1·MD·Qiangshengxing Enterprise Co., Ltd. Guishan Factory·Registered Oct 01, 2021 – Oct 31, 2023ExpiredRegistration details
- Analysis ID
- 883cfa84a0757a71492e7d7c583f9bfe
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 004679
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Qiangshengxing Enterprise Co., Ltd. Guishan Factory
Product details
- Intended Use
- Limited to the first-level identification range of the Measures for the Administration of Medical Equipment "Treatment Table (O.3520)".
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3520 treatment unit
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2023
About this record
Access comprehensive regulatory information for “Joson Care”Plinth (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 883cfa84a0757a71492e7d7c583f9bfe and manufactured by Qiangshengxing Enterprise Co., Ltd. Guishan Factory. The authorized representative in Taiwan is Qiangshengxing Enterprise Co., Ltd. Guishan Factory.
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