"Fujifilm Film" digital fluoroscopic photography imaging device
Taiwan·Risk Class 2·FUJIFILM Healthcare Corporation Medical System Operations Group, Kashiwa·Registered Jul 20, 2022 – Jul 20, 2027Active- Analysis ID
- 5084a82499e647ee916c961b8ddcca67
- Customs Code
- DHAS5603553800
- Manufacturer Country
- Japan
- Authorized Representative
- FUJIFILM HEALTHCARE TAIWAN CO., LTD.
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1730 照相透視X光系統
- Import Information
- Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
- Registration Date
- Jul 20, 2022
- Expiry Date
- Jul 20, 2027
Access comprehensive regulatory information for "Fujifilm Film" digital fluoroscopic photography 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 5084a82499e647ee916c961b8ddcca67 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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