Taiwan FDA registration 734494ba6c1db833de5861a6deab5554
"Siemens" lipoprotein A-1 & B correction solution
TW: “西門子” 脂蛋白元A-1 & B校正液
Registration details
- Analysis ID
- 734494ba6c1db833de5861a6deab5554
- Customs Code
- DHA05603180801
Company information
- Manufacturer Country
- United Kingdom;;United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- This product is intended for in vitro diagnostic use and can be used to correct APOA1 and APO B tests using Atellica CH Analyzer.
- 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
- Nov 27, 2018
- Expiry Date
- Nov 27, 2028
About this record
Access comprehensive regulatory information for "Siemens" lipoprotein A-1 & B correction solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 734494ba6c1db833de5861a6deab5554 and manufactured by RANDOX LABORATORIES LTD.;; Siemens Healthcare Diagnostics Inc.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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