"Fujifilm film" general photographic X-ray device
Taiwan·Risk Class 2·FUJIFILM Healthcare Corporation Medical System Operations Group, Kashiwa·Registered Jul 06, 2009 – Jul 06, 2029Active- Analysis ID
- ce03865344b804d2ef1f67055fd89b72
- Customs Code
- DHAS0602003601
- Manufacturer Country
- Japan
- Authorized Representative
- FUJIFILM HEALTHCARE TAIWAN CO., LTD.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1680 固定式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 06, 2009
- Expiry Date
- Jul 06, 2029
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Access comprehensive regulatory information for "Fujifilm film" general photographic X-ray device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ce03865344b804d2ef1f67055fd89b72 and manufactured by FUJIFILM Healthcare Corporation Medical System Operations Group, Kashiwa. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FUJIFILM Healthcare Corporation Medical System Operations Group, Kashiwa, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.