Taiwan FDA registration 389c217731afac5f27eeee1991a8f4b1

"Siemens" electrolyte quality control solution (unsterilized)

TW: "西門子" 電解質品管液 (未滅菌)

Taiwan·Risk Class 1·JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Apr 01, 2016 – Apr 01, 2026Expired

Registration details

Analysis ID: 389c217731afac5f27eeee1991a8f4b1
Customs Code: DHA09401635902

Company information

Manufacturer: JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.
Manufacturer Country: United States;;Japan
Authorized Representative: SIEMENS HEALTHCARE LIMITED

Product details

Intended Use: Limited to the classification and grading management of medical equipment, quality control materials (analytical and non-analytical) (A.1660) the first level identification range.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1660 Quality control materials (analytical and non-analytical)
Import Information: Contract manufacturing;; input

Dates and status

Registration Date: Apr 01, 2016
Expiry Date: Apr 01, 2026

About this record

Access comprehensive regulatory information for "Siemens" electrolyte quality control solution (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 389c217731afac5f27eeee1991a8f4b1 and manufactured by JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

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