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In Business Since 1983 !
ISO    
13485:2003   
KAMIYA BIOMEDICAL COMPANY is an ISO 13485:2003 Certified Company. Most of our diagnostic products are CE Marked and readily available for use in clinical labs all over the world!

K-Assay
 
Clinical Diagnostics
Liquid Immunoassay Reagents
 
Serum/Urine FDP-E
Method: Immunoturbidimetric
Format: Liquid
Linearity: Serum : 22 - 1,920 ng/mL (or value of highest calibrator)

Urine : 6 - 192 ng/mL (or value of highest calibrator)
Sample: Serum, Urine

For Research Use Only in the U.S.


Reagent
Cat. No. Description
KAI-113+
Serum/Urine FDP-E
    R1:   2 X 13 mL buffer
    R2:   1 X 5 mL antibody

    Tests / Kit (Hitachi 917):
    Serum: 125
    Urine: 156
    (Can Vary Based On Analyzer Model)
    
KAI-113
Click Image To Enlarge       


Recommended Calibrator
Cat. No. Description
KAI-114C+
Serum/Urine FDP-E Calibrator
6 levels prepared from lyophilized stock + diluent

5 vials of lyophilized stock and 40 mL of diluent included with kit
    
KAI-114C   Click Image To Enlarge       


Optional Sample Diluent (for high concentration urine samples)
Cat. No. Description
KAI-109D+
Urine FDP Sample Diluent
1 x 40 mL
    
KAI-109D   Click Image To Enlarge       


Recommended Controls
Cat. No. Description
K104C-10M+
Coagulation Control
5 x 2 levels, lyophilized
    
K104C-10M   Click Image To Enlarge       


Products Marked With + : For research use only in the U.S.  Not for use in diagnostic procedures in the U.S.


12779 Gateway Drive, Seattle, WA 98168, USA  •  Tel: (206) 575-8068  •  Fax: (206) 575-8094  •  E-mail: info@k-assay.com