Fujifilm Automatic Dry Biochemical Analyzer (Unsterilized)
Taiwan·Risk Class 1·FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office·Registered Oct 01, 2021 – Oct 31, 2026Active- Analysis ID
- 0a0e55533a884120f97b0ef90cdcf379
- Customs Code
- DHA08402256702
- Manufacturer Country
- Japan
- Authorized Representative
- HUNG CHONG CORP.
- Intended Use
- Limited to the first level identification range of the "Individual Photometric Chemistry Analyzer for Clinical Use (A.2160)" of the Measures for the Classification and Grading 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
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
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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 0a0e55533a884120f97b0ef90cdcf379 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office. 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 IMAGING SYSTEMS (SUZHOU) CO., LTD., 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.