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VenoFlow™ ABC AutoRetract™ safety IV cannula with Blood Control function

Automatic needle safety ánd no blood exposure!
VenoFlow™ ABC AutoRetract™ safety IV cannula with Blood Control function

Product description

The VenoFlow™ ABC AutoRetract™ safety IV cannula is designed to prevent blood leakage from the catheter hub after the IV cannula has been inserted. Due to the unique Blood Control function, it is not necessary to occlude the blood vessel when withdrawing the needle and connecting the intravenous connections. Moreover, you don't have to worry anymore about blood leakage, potentially exposing you to blood. Only when the necessary intravenous connection has been made, the flow will start. The Blood Control function continues to function even after repeated removal and connection of devices to the catheter hub.

In addition, the VenoFlow™ ABC AutoRetract™ is equipped with an automatic needle safety mechanism. The needle is automatically retracted into the safety sleeve by means of a spring mechanism. Activation of this mechanism takes place by using a push button. This automatic function allows in-vein activation, during which the needle is retracted in a straight movement and immediately permanently shielded. If a manual needle safety mechanism is preferred, we recommend the VenoFlow™ ABC Retract™ safety IV cannula from our range.

In addition to the above innovative features, the VenoFlow™ ABC AutoRetract™ meets all the usual features, such as:

  • PUR cannula for optimal performance in the vessel
  • Universally color coded
  • Available with and without fixation wings
  • Equipped with a flashback notch at the needle tip for visual confirmation of successful puncture

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Product information

Color Universally color coded
Size See product table
Product code See product table
Unit of Measure BOX/4x50
Productsheet Download PDF

Specifications

CE-markering Single use Don't use when packaging appears damaged Storage temperature Avoid direct sunlight Store in a dry environment Sterile
Classification

Medical Device class IIa

Certification
  • Manufactured according to ISO 13485:2016
  • EU Declaration of Conformity (MDR)
  • CE Certificate (MDR)
Material Multiple
Norms
  • Free of DEHP/PHT
  • Latex-free
  • BPA-free
Applications

This product has a specific medical application and should only be used in supervised setting and by authorised and able medical professionals. 

Packaging information Sterile individually packed, and then per 50 blisters in a shelf box. In an export carton, 4 shelf boxes are packed (BOX/4x50).