Fujifilm Automatic Dry Biochemical Analyzer (Unsterilized)
Taiwan·Risk Class 1·FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE·Registered Mar 11, 2015 – Mar 11, 2025Cancelled- Analysis ID
- 605d0c4ce563bf6075bc429695afcc96
- Customs Code
- DHA09401499303
- Manufacturer Country
- Japan
- Authorized Representative
- HUNG CHONG CORP.
- Intended Use
- Limited to the first level identification range of the "Individual Photometric Chemical Analyzer for Clinical Use (A.2160)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2160 Individual Photometric Chemistry Analyzer for Clinical Use
- Import Information
- Input;; QMS/QSD
- Registration Date
- Mar 11, 2015
- Expiry Date
- Mar 11, 2025
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for Fujifilm Automatic Dry Biochemical Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 605d0c4ce563bf6075bc429695afcc96 and manufactured by FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE. The authorized representative in Taiwan is HUNG CHONG CORP..
This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE, FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office, 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.