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Qizhe cardiomyogen in vitro reagent group - Taiwan Registration b211fd5c8be441579b909748183795a4

Access comprehensive regulatory information for Qizhe cardiomyogen in vitro reagent group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b211fd5c8be441579b909748183795a4 and manufactured by Longteng Biotechnology Co., Ltd. The authorized representative in Taiwan is Qizhe Biotechnology Co., Ltd.

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b211fd5c8be441579b909748183795a4
Registration Details
Taiwan FDA Registration: b211fd5c8be441579b909748183795a4
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Device Details

Qizhe cardiomyogen in vitro reagent group
TW: ๅ•Ÿๅ“ฒๅฟƒ่‚Œ็ด ้ซ”ๅค–่ฉฆๅŠ‘็ต„
Risk Class 2
Cancelled

Registration Details

b211fd5c8be441579b909748183795a4

Company Information

Taiwan, Province of China

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;; Contract manufacturing

Dates and Status

Jan 07, 2014

Dec 07, 2016

Apr 25, 2018

Cancellation Information

Logged out

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