"Siemens" therapeutic drug monitoring corrector
Taiwan·Risk Class 2·RANDOX LABORATORIES LTD.;; Siemens Healthcare Diagnostics Inc.·Registered Sep 07, 2018 – Sep 07, 2028Active- Analysis ID
- 74611e8918ba702a9f9c9e891b00008b
- Customs Code
- DHA05603145902
- Manufacturer Country
- United Kingdom;;United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
- Intended Use
- This product is used for in vitro diagnostic use and can be used in Atellica CH Analyzer for Dgn test correction.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.3200 Clinical Toxicology Corrector
- Import Information
- import
- Registration Date
- Sep 07, 2018
- Expiry Date
- Sep 07, 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 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.