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"Dinax" Diess Clinical use enzyme analyzer (unsterilized) - Taiwan Registration 30ee8748dff6cd951b5cea3e379a69fc

Access comprehensive regulatory information for "Dinax" Diess 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 30ee8748dff6cd951b5cea3e379a69fc and manufactured by DYNEX TECHNOLOGIES INC.. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health 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.

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30ee8748dff6cd951b5cea3e379a69fc
Registration Details
Taiwan FDA Registration: 30ee8748dff6cd951b5cea3e379a69fc
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Device Details

"Dinax" Diess Clinical use enzyme analyzer (unsterilized)
TW: โ€œ่ฟชๅฅˆๅ…‹ๆ–ฏโ€่ฟชๆ–ฏ ่‡จๅบŠไฝฟ็”จ้…ต็ด ๅˆ†ๆžๅ„€(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

30ee8748dff6cd951b5cea3e379a69fc

DHA04401283100

Company Information

United States

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

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Mar 22, 2013

Mar 22, 2023

Sep 30, 2021

Cancellation Information

Logged out

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