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Primus Ultra2 Variant Analyzer with Model 215 Auto-Sampler(Non-Sterile) - Taiwan Registration 68c40d99f1632eb274be12188f71ab79

Access comprehensive regulatory information for Primus Ultra2 Variant Analyzer with Model 215 Auto-Sampler(Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 68c40d99f1632eb274be12188f71ab79 and manufactured by Trinity Biotech (Primus Corporation dba Trinity Biotech). The authorized representative in Taiwan is PROGRESSIVE GROUP INC..

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68c40d99f1632eb274be12188f71ab79
Registration Details
Taiwan FDA Registration: 68c40d99f1632eb274be12188f71ab79
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Device Details

Primus Ultra2 Variant Analyzer with Model 215 Auto-Sampler(Non-Sterile)
TW: 普林莫斯優特二型全自動化高壓液相層析儀(未滅菌)
Risk Class 1
MD

Registration Details

68c40d99f1632eb274be12188f71ab79

Ministry of Health Medical Device Import Registration No. 003152

DHA08400315202

Company Information

Product Details

A device that separates one or more drugs or compounds from a solution.

A Clinical chemistry and clinical toxicology

A2260 High pressure liquid chromatograph for clinical use

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026