Taiwan FDA registration 5a7e38384dcac9d70babed30d2c8c5f8
"Fujifilm" mobile digital X-ray system
TW: “富士” 移動式數位X光透視系統
Taiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office;; FUJIFILM CORPORATION·Registered Jul 01, 2023 – Jul 01, 2028ActiveRegistration details
- Analysis ID
- 5a7e38384dcac9d70babed30d2c8c5f8
- Customs Code
- DHAS5603655900
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- FUJIFILM HEALTHCARE TAIWAN CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1720 移動式X光系統
- Import Information
- Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input
Dates and status
- Registration Date
- Jul 01, 2023
- Expiry Date
- Jul 01, 2028
About this record
Access comprehensive regulatory information for "Fujifilm" mobile digital X-ray system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5a7e38384dcac9d70babed30d2c8c5f8 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office;; FUJIFILM CORPORATION. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..
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