Taiwan FDA registration e1ba30fcf920d420fc5e40b9fc8ff708
“Microtek” Medical X-Ray Digitizer
TW: “全友”醫用X光片數位儀
Taiwan·Risk Class 2·MD·MICROTEK INTERNATIONAL INC.·Registered Jan 25, 2017 – Jan 25, 2027ActiveRegistration details
- Analysis ID
- e1ba30fcf920d420fc5e40b9fc8ff708
- License Form
- Ministry of Health Medical Device Manufacturing No. 005654
Company information
- Manufacturer
- MICROTEK INTERNATIONAL INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- MICROTEK INTERNATIONAL INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P2050 Medical Image Management and Processing System
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jan 25, 2017
- Expiry Date
- Jan 25, 2027
About this record
Access comprehensive regulatory information for “Microtek” Medical X-Ray Digitizer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e1ba30fcf920d420fc5e40b9fc8ff708 and manufactured by MICROTEK INTERNATIONAL INC.. The authorized representative in Taiwan is MICROTEK INTERNATIONAL INC..
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