Taiwan FDA registration afe44bea090ba1e996db9439d463f8ae

"Siemens" HDL/LDL cholesterol correction solution

TW: “西門子” HDL/LDL 膽固醇校正液

Taiwan·Risk Class 2·RANDOX LABORATORIES LTD.;; Siemens Healthcare Diagnostics Inc.·Registered Nov 02, 2018 – Nov 02, 2028Active

Registration details

Analysis ID: afe44bea090ba1e996db9439d463f8ae
Customs Code: DHA05603177305

Company information

Manufacturer: RANDOX LABORATORIES LTD.;; Siemens Healthcare Diagnostics Inc.
Manufacturer Country: United Kingdom;;United States
Authorized Representative: SIEMENS HEALTHCARE LIMITED

Product details

Intended Use: This product is intended for in vitro diagnostic use to calibrate the Atellica CH analyzer during D-HDL and DLDL tests.
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 02, 2018
Expiry Date: Nov 02, 2028

About this record

Access comprehensive regulatory information for "Siemens" HDL/LDL cholesterol 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 afe44bea090ba1e996db9439d463f8ae and manufactured by RANDOX LABORATORIES LTD.;; Siemens Healthcare Diagnostics Inc.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

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