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"Dynax" Enzyme Analyzer for Clinical Use (Unsterilized) - Taiwan Registration d333c9c0bbaac3e185515589fd873186

Access comprehensive regulatory information for "Dynax" Enzyme Analyzer for Clinical Use (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d333c9c0bbaac3e185515589fd873186 and manufactured by DYNEX TECHNOLOGIES INC.. The authorized representative in Taiwan is MEDTRI CO., LTD..

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.

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d333c9c0bbaac3e185515589fd873186
Registration Details
Taiwan FDA Registration: d333c9c0bbaac3e185515589fd873186
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Device Details

"Dynax" Enzyme Analyzer for Clinical Use (Unsterilized)
TW: "ๅฒฑๅฅˆๅ…‹ๅธ" ่‡จๅบŠไฝฟ็”จ้…ต็ด ๅˆ†ๆžๅ„€ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

d333c9c0bbaac3e185515589fd873186

DHA08402265305

Company Information

United States

Product Details

Limited to the classification and grading management measures of medical equipment "Enzyme Analyzer for Clinical Use (A.2500)" first level identification range.

A Clinical chemistry and clinical toxicology

A.2500 Enzyme analyzer for clinical use

Input;; QMS/QSD

Dates and Status

Oct 01, 2021

Oct 31, 2026

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