Taiwan FDA registration faa9f1c9af2914ba27bc34c78e62181e

"Siemens" microalbumin corrector

TW: “西門子”微量白蛋白校正品

Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.·Registered Sep 19, 2008 – Sep 19, 2013Cancelled

Registration details

Analysis ID: faa9f1c9af2914ba27bc34c78e62181e
Customs Code: DHA00601944306

Company information

Manufacturer: SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.
Manufacturer Country: United Kingdom;;United States
Authorized Representative: SIEMENS LIMITED

Product details

Intended Use: It is used to calibrate the ADVIA biochemical analysis system for the detection of microalbumin in extremity diagnostic tests.
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: Sep 19, 2008
Expiry Date: Sep 19, 2013
Cancellation Date: Aug 10, 2015

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Siemens" microalbumin corrector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number faa9f1c9af2914ba27bc34c78e62181e and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is SIEMENS LIMITED.

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