"Siemens" therapeutic drug monitoring corrector
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.·Registered Jul 01, 2008 – Jul 01, 2028Active- Analysis ID
- 9683e8f49b74661310349c268eb4dc35
- Customs Code
- DHA00601939801
- Manufacturer Country
- United Kingdom;;United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
- Intended Use
- In vitro diagnostic test for the detection of therapeutic drugs by the ADVIA biochemical analysis system.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.3200 Clinical Toxicology Corrector
- Import Information
- import
- Registration Date
- Jul 01, 2008
- Expiry Date
- Jul 01, 2028
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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.