Taiwan FDA registration 5b6ee0bafda516757544051861c000f4

"Siemens" urine total protein correction solution

TW: “西門子” 尿液總蛋白校正液

Taiwan·Risk Class 2·RANDOX LABORATORIES LTD.;; Siemens Healthcare Diagnostics Inc.·Registered Oct 31, 2018 – Oct 31, 2028Active

Registration details

Analysis ID: 5b6ee0bafda516757544051861c000f4
Customs Code: DHA05603176901

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 used for calibration during Atellica CH Analyzer UPro analysis.
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: Oct 31, 2018
Expiry Date: Oct 31, 2028

About this record

Access comprehensive regulatory information for "Siemens" urine total protein 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 5b6ee0bafda516757544051861c000f4 and manufactured by RANDOX LABORATORIES LTD.;; Siemens Healthcare Diagnostics Inc.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

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