"Fujifilm" digital X-ray photography system
Taiwan·Risk Class 2·FUJIFILM TECHNO PRODUCTS CO., LTD. TOUHOKU FACTORY HANAMAKI SITE·Registered Feb 09, 2011 – Feb 09, 2021Cancelled- Analysis ID
- d892b9eeca45f4b958f24a2f63b76cdf
- Customs Code
- DHA00602205303
- 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.1630 靜電式X光影像系統
- Import Information
- import
- Registration Date
- Feb 09, 2011
- Expiry Date
- Feb 09, 2021
- Cancellation Date
- Sep 19, 2023
- Status
- Logged out
- Reason
- 自行鍵入
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Access comprehensive regulatory information for "Fujifilm" digital X-ray photography system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d892b9eeca45f4b958f24a2f63b76cdf and manufactured by FUJIFILM TECHNO PRODUCTS CO., LTD. TOUHOKU FACTORY HANAMAKI SITE. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including FUJIFILM Corporation;; FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office, FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office;; FUJIFILM CORPORATION, and 5 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.