Taiwan FDA registration 2f43378c995f0e51de0f3d27b7ca1e24
"DIVA" Medical image communication device (Non-Sterile)
TW: "鈺緯" 醫學影像傳輸裝置 (未滅菌)
Taiwan·Risk Class 1·MD·DIVA LABORATORIES, LTD.·Registered Mar 16, 2017 – Mar 16, 2022ExpiredRegistration details
- Analysis ID
- 2f43378c995f0e51de0f3d27b7ca1e24
- License Form
- Ministry of Health Medical Device Manufacturing No. 006634
Company information
- Manufacturer
- DIVA LABORATORIES, LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- DIVA LABORATORIES, LTD.
Product details
- Intended Use
- Limited to the first-level recognition range of medical image transmission devices (P.2020) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P2020 Medical Image Transmission Device
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Mar 16, 2017
- Expiry Date
- Mar 16, 2022
About this record
Access comprehensive regulatory information for "DIVA" Medical image communication device (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 2f43378c995f0e51de0f3d27b7ca1e24 and manufactured by DIVA LABORATORIES, LTD.. The authorized representative in Taiwan is DIVA LABORATORIES, LTD..
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