KINDER DL™ double-lumen aspiration device, allowing simultaneous or intermittent flushing of media and follicular fluid aspiration for efficient oocyte retrieval

KINDER DL™

Double lumen oocyte aspiration needle

Double-lumen aspiration device, allowing simultaneous or intermittent flushing of media and follicular fluid aspiration for efficient oocyte retrieval.
  • Diagnosi prenatale
  • Direct connection between needle and aspiration line;
  • Ergonomic grip with thumb notch to indicate the orientation of the tip;
  • Echo markings for accurate placement under ultrasound guidance;
  • Triple cut tip to reduce trauma;
  • Different measures available upon request.

Oocyte retrieval is a crucial step in Assisted Reproduction Technology (ART), involving the collection of eggs from ovarian follicles. A double-lumen aspiration needle enhances this procedure by allowing both follicular fluid aspiration and controlled flushing of culture media, improving oocyte recovery rates.

Under ultrasound guidance, the needle is inserted into the ovarian follicles. The first lumen is used for aspiration, drawing out the follicular fluid containing the oocyte, while the second lumen enables the injection of a flushing medium. This medium helps detach oocytes that may still be adhered to the follicle wall, increasing the chances of successful retrieval. Depending on the clinician’s preference, the flushing and aspiration can be performed simultaneously or intermittently.

This design ensures greater efficiency and precision, optimizing the number of viable oocytes collected while minimizing trauma to the ovarian tissue.

GAUGE DIAMETER (mm) PRODUCT CODE Needle Length (cm) PIECES PER BOX
16G 1,60 KKN2V1635E8090 35 10
17G 1,47 KKN2V1735E8090 35 10

RELATED PRODUCTs

Single lumen oocyte aspiration needle

Fill out the form below, one of our expert will get in touch with you shortly!

Notice reserved for healthcare professionals

The content of this website is intended exclusively for healthcare professionals.
In accordance with current regulations (Legislative Decree 46/97 and EU Regulation 2017/745), access to information related to medical devices is restricted to healthcare professionals only.

I declare that I am a healthcare professional.