"Fujifilm" medical dry image printer
Taiwan·Risk Class 2·FUJIFILM IMAGING SYSTEMS (SUZHOU) CO., LTD.;; FUJIFILM CORPORATION·Registered Oct 16, 2013 – Oct 16, 2028Active- Analysis ID
- 6a2c054e57ef56b151ecb1f53c86a6b5
- Customs Code
- DHA09200054907
- Manufacturer Country
- Japan;;China
- 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.2040 醫學影像列印裝置
- Import Information
- Chinese goods;; Contract manufacturing;; input
- Registration Date
- Oct 16, 2013
- Expiry Date
- Oct 16, 2028
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Access comprehensive regulatory information for "Fujifilm" medical dry image printer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6a2c054e57ef56b151ecb1f53c86a6b5 and manufactured by FUJIFILM IMAGING SYSTEMS (SUZHOU) CO., LTD.;; FUJIFILM CORPORATION. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including FUJIFILM IMAGING SYSTEMS (SUZHOU) CO., LTD.;; FUJIFILM CORPORATION, FUJIFILM TECHNO PRODUCTS CO., LTD. TOUHOKU FACTORY HANAMAKI SITE, and 3 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.