Taiwan FDA registration 489568316334dd442255f8ffc669bff4
"Siemens" second-generation calcium reagent group
TW: “西門子”第二代鈣試劑組
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.·Registered Mar 11, 2009 – Mar 11, 2029ActiveRegistration details
- Analysis ID
- 489568316334dd442255f8ffc669bff4
- Customs Code
- DHA00601996306
Company information
- Manufacturer Country
- United Kingdom;;United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- Quantitative determination of calcium in human serum, plasma and urine.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1145 Calcium Test System
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Mar 11, 2009
- Expiry Date
- Mar 11, 2029
About this record
Access comprehensive regulatory information for "Siemens" second-generation calcium reagent group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 489568316334dd442255f8ffc669bff4 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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