Taiwan FDA registration 844817719e175bd6d810cb44a2b181aa

"Demanson" Chemical Corrective Reagent II

TW: "德曼遜" 化學校正試劑II

Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS·Registered Apr 17, 2006 – Apr 17, 2026Expired

Registration details

Analysis ID: 844817719e175bd6d810cb44a2b181aa
Customs Code: DHA00601636306

Company information

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

Product details

Intended Use: In vitro diagnostic reagents for calibration of magnesium (MG), phosphorus (PHOS), and triglycerides (TRIG) assays on the dermanson clinical chemistry system.
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: Apr 17, 2006
Expiry Date: Apr 17, 2026

About this record

Access comprehensive regulatory information for "Demanson" Chemical Corrective Reagent II in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 844817719e175bd6d810cb44a2b181aa and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

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