Taiwan FDA registration 375f9d95c707ed92d494b21758806810

"Siemens" electrolyte relief solution

TW: “西門子”電解質緩解液

Taiwan·Risk Class 2·JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Mar 02, 2009 – Mar 02, 2029Active

Registration details

Analysis ID: 375f9d95c707ed92d494b21758806810
Customs Code: DHA00601995902

Company information

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

Product details

Intended Use: It is used to quantitatively measure the concentration of electrolytes in human serum, plasma and urine in the Siemens ADVIA chemical system. Performance change: Used in the Siemens ADVIA 1800/2400 chemical system to quantitatively measure the concentration of electrolytes in human serum, plasma and urine.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1150 Calibrated Products
Import Information: Input;; Contract manufacturing

Dates and status

Registration Date: Mar 02, 2009
Expiry Date: Mar 02, 2029

About this record

Access comprehensive regulatory information for "Siemens" electrolyte relief solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 375f9d95c707ed92d494b21758806810 and manufactured by JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

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