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Longteng cardiomyocardin in vitro reagent card (serum) - Taiwan Registration 903118cda4abeef833aca9714d00ba89

Access comprehensive regulatory information for Longteng cardiomyocardin in vitro reagent card (serum) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 903118cda4abeef833aca9714d00ba89 and manufactured by The first factory of Longteng Biotechnology Co., Ltd. The authorized representative in Taiwan is The first factory of Longteng Biotechnology Co., 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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903118cda4abeef833aca9714d00ba89
Registration Details
Taiwan FDA Registration: 903118cda4abeef833aca9714d00ba89
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Device Details

Longteng cardiomyocardin in vitro reagent card (serum)
TW: ้พ้จฐๅฟƒ่‚Œ็ด ้ซ”ๅค–่ฉฆๅŠ‘ๅก(่ก€ๆธ…)
Risk Class 2
Cancelled

Registration Details

903118cda4abeef833aca9714d00ba89

DHY00500228903

Company Information

Product Details

Qualitative detection of Troponin I antibodies in human serum.

A Clinical chemistry and clinical toxicology

A.1215 Creatine phosphokinase/creatine kinase or isoenzyme testing system

Domestic

Dates and Status

Dec 07, 2006

Dec 07, 2016

Dec 13, 2019

Cancellation Information

Logged out

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