"Siemens" C-reactive protein corrector - Taiwan Registration a0c32a44cc296916c20ce9e5861487d6
Access comprehensive regulatory information for "Siemens" C-reactive protein corrector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a0c32a44cc296916c20ce9e5861487d6 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is SIEMENS LIMITED.
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.
Device Details
Registration Details
a0c32a44cc296916c20ce9e5861487d6
DHA00601942708
Product Details
In vitro diagnostic test for the detection of C-reactive protein by the calibration ADVIA biochemical analysis system.
A Clinical chemistry and clinical toxicology
A.1150 Calibrated Products
import
Dates and Status
Aug 22, 2008
Aug 22, 2013
Aug 10, 2015
Cancellation Information
Logged out
่จฑๅฏ่ญๅทฒ้พๆๆๆ