Sanmeng urea liquid test system - Taiwan Registration dab724ab20e8d39fc26fa810f074e5c7
Access comprehensive regulatory information for Sanmeng urea liquid test system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dab724ab20e8d39fc26fa810f074e5c7 and manufactured by FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A SUBSIDIARY OF THERMO FISHER. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..
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Device Details
Product Details
It is used to quantify urea in human serum, blood or urine in vitro
A Clinical chemistry and clinical toxicology
A.1770 ๅฐฟ็ด ๆฐฎ่ฉฆ้ฉ็ณป็ตฑ
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Dates and Status
Dec 18, 2009
Dec 18, 2014
Apr 25, 2018
Cancellation Information
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