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CMA 64 IView Microdialysis Catheter

   

 

 

    Continuous intravenous monitoring of
     substances in the blood for up to 3 days

    Easy insertion using a standard peripheral
      venous catheter

    Unique membrane characteristics optimize 

    

 Product note (pdf)

CMA 64 IView Microdialysis Catheter

The CMA 64 IView Microdialysis Catheter is a sterile, single use device intended for intravenous monitoring through a standard peripheral vein catheter (PVC) up to 72 hours. The clean samples and possibility for frequent sampling makes it ideal for research.

Small substances diffuse into the IView catheter reflecting accurate concentrations in blood. It is perfused with a physiologic solution, containing the anticoagulant dalteparin sodium, to avoid clotting. The samples are collected in Microvials and can be analyzed as often as every minute. The catheter forms a complete system together with the CMA 107 Microdialysis Pump and the ISCUSflex Microdialysis Analyzer.

The catheter is also excellent for continuously monitoring the free fractions of drugs in blood during pharmacokinetic and pharmacodynamic studies.

Technical information for CMA 64 IView

Membrane Cut-off: Approx. 20,000 Daltons
Membrane characteristics: The IView membrane has a very smooth outer surface especially developed for use in blood.
Material Length (mm)
8010520 		Length (mm)
8010521 		Length (mm)
8010830 		Diameter
(mm)
Shaft Polyurethane   46   46   46 0.9
Membrane PAES *   10   20   30 0.6
Inlet Tubing Polyurethane 200 200 200 1.0
Outlet Tubing Polyurethane   45   45   45 1.0
* PAES = Polyarylethersulphone 
           

Ordering information for CMA 64 IView

     

Ref. No.
8010520 IView CMA 64 Catheter 46/10, 4/pkg, including Introducer **
8010521 IView CMA 64 Catheter 46/20, 4/pg, including Introducer
8010830 IView CMA 64 Catheter 46/30, 4/pg, including Introducer

Accessories:
P000001 Microvials
P000028 Microvials in Rack
P000154 Microvials in Rack Sterile  

  **Only produced by order

NOTE: This product may not be approved by your national regulatory authorities.
Please contact your local CMA representative for further information.