Fuji Dry Immunoassay Analyzer (Unsterilized) - Taiwan Registration 0c5a07be51f8e8922215a175e71f399a
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.
Device Details
Product Details
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.
A Clinical chemistry and clinical toxicology
A.2300 Colorimeter, photometer, or spectrophotometer for clinical use
Contract manufacturing;; input
Dates and Status
May 02, 2018
May 02, 2023
Sep 30, 2021
Cancellation Information
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