"Siemens" therapeutic drug monitoring corrector - Taiwan Registration 9683e8f49b74661310349c268eb4dc35
Access comprehensive regulatory information for "Siemens" therapeutic drug monitoring corrector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9683e8f49b74661310349c268eb4dc35 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including RANDOX LABORATORIES LTD.;; Siemens Healthcare Diagnostics Inc., and 1 recent registrations in the same category. 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
9683e8f49b74661310349c268eb4dc35
DHA00601939801
Product Details
In vitro diagnostic test for the detection of therapeutic drugs by the ADVIA biochemical analysis system.
A Clinical chemistry and clinical toxicology
A.3200 Clinical Toxicology Corrector
import
Dates and Status
Jul 01, 2008
Jul 01, 2028