"Siemens" therapeutic drug monitoring corrector - Taiwan Registration 74611e8918ba702a9f9c9e891b00008b
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 74611e8918ba702a9f9c9e891b00008b and manufactured by RANDOX LABORATORIES LTD.;; Siemens Healthcare Diagnostics Inc.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD., 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
74611e8918ba702a9f9c9e891b00008b
DHA05603145902
Product Details
This product is used for in vitro diagnostic use and can be used in Atellica CH Analyzer for Dgn test correction.
A Clinical chemistry and clinical toxicology
A.3200 Clinical Toxicology Corrector
import
Dates and Status
Sep 07, 2018
Sep 07, 2028