Taiwan FDA registration dac213b43d606a3143c945db626f276b

"Siemens" calcium analysis reagent set

TW: “西門子” 鈣分析試劑組

Taiwan·Risk Class 2·RANDOX LABORATORIES LTD.;; Siemens Healthcare Diagnostics Inc.·Registered Aug 28, 2018 – Aug 28, 2028Active

Registration details

Analysis ID: dac213b43d606a3143c945db626f276b
Customs Code: DHA05603143906

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 in vitro diagnostic use with Atellica CH Analyzer to quantitatively detect calcium in human serum, plasma (heparin lithium) and urine.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1145 Calcium Test System
Import Information: import

Dates and status

Registration Date: Aug 28, 2018
Expiry Date: Aug 28, 2028

About this record

Access comprehensive regulatory information for "Siemens" calcium analysis reagent set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dac213b43d606a3143c945db626f276b and manufactured by RANDOX LABORATORIES LTD.;; Siemens Healthcare Diagnostics Inc.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

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