"Fujifilm" medical dry image printer and its accessories
Taiwan·Risk Class 2·FUJIFILM TECHNO PRODUCTS CO., LTD. TOUHOKU FACTORY HANAMAKI SITE·Registered Sep 24, 2008 – Sep 24, 2018Cancelled- Analysis ID
- 163aa3e5df0500a9a8fc292bff72bba6
- Customs Code
- DHA00601922700
- Manufacturer Country
- Japan
- Authorized Representative
- NAN KAI CORPORATION
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- P Radiology Science
- Import Information
- import
- Registration Date
- Sep 24, 2008
- Expiry Date
- Sep 24, 2018
- Cancellation Date
- Jun 22, 2022
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Fujifilm" medical dry image printer and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 163aa3e5df0500a9a8fc292bff72bba6 and manufactured by FUJIFILM TECHNO PRODUCTS CO., LTD. TOUHOKU FACTORY HANAMAKI SITE. The authorized representative in Taiwan is NAN KAI CORPORATION.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FUJIFILM IMAGING SYSTEMS (SUZHOU) CO., LTD.;; FUJIFILM CORPORATION, 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.