Taiwan FDA registration ec7efd01982d088856488f9c8fa2948d
"Demanson" iron correction reagent
TW: “德曼遜”鐵校正試劑
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS·Registered Apr 08, 2010 – Apr 08, 2030ActiveRegistration details
- Analysis ID
- ec7efd01982d088856488f9c8fa2948d
- Customs Code
- DHA00602096500
Company information
- Manufacturer Country
- United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- The IRON Calibration Reagent is an in vitro diagnostic reagent used to correct iron (IRON) detection on the Dimension® 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 08, 2010
- Expiry Date
- Apr 08, 2030
About this record
Access comprehensive regulatory information for "Demanson" iron correction reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ec7efd01982d088856488f9c8fa2948d and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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