"Pusen" Qiwei Clinical use enzyme analyzer (unsterilized) - Taiwan Registration 033e6638ca1ee7b79547ec28ac7c4e0a
Access comprehensive regulatory information for "Pusen" Qiwei Clinical use enzyme 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 033e6638ca1ee7b79547ec28ac7c4e0a and manufactured by DYNEX TECHNOLOGIES INC.. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DYNEX TECHNOLOGIES INC., 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 enzyme analyzer for clinical use (A.2500) of the Measures for the Administration of Medical Devices.
A Clinical chemistry and clinical toxicology
A.2500 Enzyme analyzer for clinical use
Input;; QMS/QSD
Dates and Status
Oct 02, 2013
Oct 02, 2023
Sep 30, 2021
Cancellation Information
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