Fuji Dry Immunoassay Analyzer (Unsterilized)
Taiwan·Risk Class 1·TERASAKI ELECTRIC CO., LTD. SYSTEM DIV. YAO FACTORY;; FUJIFILM CORPORATION·Registered Oct 01, 2021 – Oct 31, 2023Cancelled- Analysis ID
- 29eea5709d06638fafa1fce0009dbcae
- Customs Code
- DHA08401901604
- Manufacturer Country
- Japan
- Authorized Representative
- ISIN INC.
- Intended Use
- Limited to the first level identification range of the Measures for the Classification and Grading of Medical Devices "Colorimeter, Photometer or Spectrophotometer for Clinical Use (A.2300)".
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2300 Colorimeter, photometer, or spectrophotometer for clinical use
- Import Information
- Contract manufacturing;; input
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2023
- Cancellation Date
- Nov 02, 2023
- Status
- Logged out
- Reason
- 未展延而逾期者
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Access comprehensive regulatory information for Fuji Dry Immunoassay 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 29eea5709d06638fafa1fce0009dbcae and manufactured by TERASAKI ELECTRIC CO., LTD. SYSTEM DIV. YAO FACTORY;; FUJIFILM CORPORATION. The authorized representative in Taiwan is ISIN INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TERASAKI ELECTRIC CO., LTD. SYSTEM DIV. YAO FACTORY;; 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.