Taiwan FDA registration f23a874681fc85166c7ea2bb6181e249

Vitex 350 Chemical Analyzer (Unsterilized)

TW: 〝維特司〞350化學分析儀(未滅菌)
Taiwan flagTaiwan·Risk Class 1·NPA DE MEXICO S. DE R.L. DE C.V.;; ORTHO-CLINICAL DIAGNOSTICS, INC·Registered Oct 01, 2021 – Oct 31, 2025Expired
Registration details
Analysis ID
f23a874681fc85166c7ea2bb6181e249
Customs Code
DHA08400078207
Company information
Manufacturer Country
Mexico;;United States
Authorized Representative
DKSH TAIWAN LTD.
Product details
Intended Use
Clinical biochemical project test analysis.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.2160 Individual Photometric Chemistry Analyzer for Clinical Use
Import Information
Contract manufacturing;; input
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2025
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About this record

Access comprehensive regulatory information for Vitex 350 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 f23a874681fc85166c7ea2bb6181e249 and manufactured by NPA DE MEXICO S. DE R.L. DE C.V.;; ORTHO-CLINICAL DIAGNOSTICS, INC. The authorized representative in Taiwan is DKSH TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including NPA DE MEXICO S. DE R.L. DE C.V.;; ORTHO-CLINICAL DIAGNOSTICS, 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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