Fuji Dry Immunoassay Analyzer (Unsterilized)
Taiwan·Risk Class 1·TERASAKI ELECTRIC CO., LTD. SYSTEM DIV. YAO FACTORY;; FUJIFILM CORPORATION·Registered May 02, 2018 – May 02, 2023Cancelled- Analysis ID
- 0c5a07be51f8e8922215a175e71f399a
- Customs Code
- DHA09401901600
- Manufacturer Country
- Japan
- Authorized Representative
- ISIN INC.
- Intended Use
- Limited to the first level identification range of "Colorimeter, Photometer or Spectrophotometer for Clinical Use (A.2300)" under the Measures for the Administration of Medical Devices.
- 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
- May 02, 2018
- Expiry Date
- May 02, 2023
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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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 0c5a07be51f8e8922215a175e71f399a 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.