Taiwan FDA registration 82949facd2885e50607b836d08def1bd
"Fujifilm Film" MRI imaging device
TW: “富士軟片”核磁共振影像裝置
Taiwan·Risk Class 2·FUJIFILM Healthcare Corporation Medical System Operations Group, Kashiwa·Registered May 21, 2004 – May 21, 2029ActiveRegistration details
- Analysis ID
- 82949facd2885e50607b836d08def1bd
- Customs Code
- DHA00601066100
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- FUJIFILM HEALTHCARE TAIWAN CO., LTD.
Product details
- Product Type (Level 1)
- P Radiology Science
- Import Information
- import
Dates and status
- Registration Date
- May 21, 2004
- Expiry Date
- May 21, 2029
About this record
Access comprehensive regulatory information for "Fujifilm Film" MRI imaging device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 82949facd2885e50607b836d08def1bd and manufactured by FUJIFILM Healthcare Corporation Medical System Operations Group, Kashiwa. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..
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