"Fujifilm Film" whole body computed tomography X-ray device
- Analysis ID
- 4e186a45af33c24f65cf9ec9b7545e6f
- Customs Code
- DHAS5603376409
- 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.1750 電腦斷層掃描X光系統
- Import Information
- Input;; Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.
- Registration Date
- Jun 15, 2020
- Expiry Date
- Jun 15, 2025
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Access comprehensive regulatory information for "Fujifilm Film" whole body computed tomography 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 4e186a45af33c24f65cf9ec9b7545e6f 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.