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"Vitex" 950 Chemical Analyzer (Unsterilized) - Taiwan Registration ffe34fd2b92d38edae32aad065b9d52a

Access comprehensive regulatory information for "Vitex" 950 Chemical 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 ffe34fd2b92d38edae32aad065b9d52a and manufactured by ORTHO-CLINICAL DIAGNOSTICS, INC. The authorized representative in Taiwan is DKSH TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details. 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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ffe34fd2b92d38edae32aad065b9d52a
Registration Details
Taiwan FDA Registration: ffe34fd2b92d38edae32aad065b9d52a
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Device Details

"Vitex" 950 Chemical Analyzer (Unsterilized)
TW: "็ถญ็‰นๅธ" 950 ๅŒ–ๅญธๅˆ†ๆžๅ„€(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

ffe34fd2b92d38edae32aad065b9d52a

DHA04400063204

Company Information

United States

Product Details

Clinical biochemical project test analysis.

A Clinical chemistry and clinical toxicology

import

Dates and Status

Sep 28, 2005

Sep 28, 2015

Aug 14, 2018

Cancellation Information

Logged out

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