Taiwan FDA registration 30050b42e9a72c7ac3d65a0df1d2b50a
“Chang Gung” Plinth (Non-Sterile)
TW: “長庚”治療檯 (未滅菌)
Taiwan·Risk Class 1·MD·Chang Gung Medical Technology Co., Ltd. Linkou Factory·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- 30050b42e9a72c7ac3d65a0df1d2b50a
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 005457
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- CHANG GUNG MEDICAL TECHNOLOGY CO., LTD.
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, 2025
About this record
Access comprehensive regulatory information for “Chang Gung” 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 30050b42e9a72c7ac3d65a0df1d2b50a and manufactured by Chang Gung Medical Technology Co., Ltd. Linkou Factory. The authorized representative in Taiwan is CHANG GUNG MEDICAL TECHNOLOGY CO., LTD..
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