Taiwan FDA registration 9794dc8feb72e074568da7ea1c1f1094

Dermanson Müster Cardiac Troponin I Flex Reagent Set

TW: 德曼遜敏斯特心肌肌鈣蛋白I弗列克斯試劑組

Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Nov 25, 2011 – Nov 25, 2016Cancelled

Registration details

Analysis ID: 9794dc8feb72e074568da7ea1c1f1094
Customs Code: DHA00602274700

Company information

Manufacturer: SIEMENS HEALTHCARE DIAGNOSTICS INC.
Manufacturer Country: United States
Authorized Representative: SIEMENS LIMITED

Product details

Intended Use: This product is used with the Dimension Vista System to measure serum and plasma centrotroponin I concentrations.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1215 Creatine phosphokinase/creatine kinase or isoenzyme testing system
Import Information: import

Dates and status

Registration Date: Nov 25, 2011
Expiry Date: Nov 25, 2016
Cancellation Date: Jul 31, 2018

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for Dermanson Müster Cardiac Troponin I Flex 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 9794dc8feb72e074568da7ea1c1f1094 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS LIMITED.

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