Taiwan FDA registration 0f6ac1e31bfcfb00d9087b15d2624d26
"Siemens" HDL/LDL cholesterol corrector
TW: “西門子”高密度脂蛋白/低密度脂蛋白膽固醇校正品
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.·Registered Jul 09, 2008 – Jul 09, 2028ActiveRegistration details
- Analysis ID
- 0f6ac1e31bfcfb00d9087b15d2624d26
- Customs Code
- DHA00601940600
Company information
- Manufacturer Country
- United Kingdom;;United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- In vitro diagnostic tests for the calibration of ADVIA biochemical analysis system for the detection of direct HDL cholesterol, HDL type II and direct LDL cholesterol.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1150 Calibrated Products
- Import Information
- import
Dates and status
- Registration Date
- Jul 09, 2008
- Expiry Date
- Jul 09, 2028
About this record
Access comprehensive regulatory information for "Siemens" HDL/LDL cholesterol corrector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0f6ac1e31bfcfb00d9087b15d2624d26 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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