Fuji Dry Immunoassay Analyzer (Unsterilized) - Taiwan Registration 29eea5709d06638fafa1fce0009dbcae
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.
Device Details
Product Details
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)".
A Clinical chemistry and clinical toxicology
A.2300 Colorimeter, photometer, or spectrophotometer for clinical use
Contract manufacturing;; input
Dates and Status
Oct 01, 2021
Oct 31, 2023
Nov 02, 2023
Cancellation Information
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