"Siemens" basic phosphoric acid per (AMP method) reagent set - Taiwan Registration e5deb9fe14acc1a6365c6b808e3b5cdf
Access comprehensive regulatory information for "Siemens" basic phosphoric acid per (AMP method) reagent set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e5deb9fe14acc1a6365c6b808e3b5cdf and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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Device Details
Registration Details
e5deb9fe14acc1a6365c6b808e3b5cdf
DHA00601893101
Product Details
For in vitro diagnostics. The activity of basic phosphoric acid in human serum and plasma was quantitatively determined on the ADVIA fully automated chemical analysis system.
A Clinical chemistry and clinical toxicology
A.1050 Alkaline phosphatase or isoenzyme testing system
import
Dates and Status
Jan 22, 2008
Jan 22, 2018
Nov 04, 2019
Cancellation Information
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