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TYSHAK Mini® Pediatric Valvuloplasty catheter

The TYSHAK Mini® Pediatric Valvuloplasty catheter has been designed and engineered with a super thin balloon of 2.0 or 4.0 cm in usable length along with a 2.5/3.5 Fr shaft and mini distal tip, making the TYSHAK Mini® the lowest profile of any available balloon in its diameter.

  • General
  • Specifications
  • Catheter Characteristics

    The TYSHAK Mini® Pediatric Valvuloplasty catheter has been designed and engineered with a super thin balloon of 2.0 or 4.0 cm in usable length along with a 2.5/3.5 Fr shaft and mini distal tip, making the TYSHAK Mini® the lowest profile of any available balloon in its diameter.

    Super Thin Balloon

    The TYSHAK Mini® Pediatric Valvuloplasty balloon is super thin for a low deflated profile that maintains tip flexibility. The exceptionally low profile balloon requires the smallest introducer possible.

    Double Tapered Balloon

    The TYSHAK Mini® Pediatric Valvuloplasty catheter has short tapers at the distal and proximal ends for enhanced transition across the stenosis and post dilatation ease of withdrawal into the introducer.

    Radiopaque marker

    Platinum marker bands facilitate reliable positioning of the balloon.

  • Product specifications

    Balloon
    Diameter
    (MM)
    Balloon
    Length
    (CM)
    Introducer
    Size
    (FR)
    Shaft
    Size
    (FR)
    Usable
    Length
    (CM)
    Guide Wire
    (Inches)
    Rated
    Burst
    (ATM)
    *Nominal
    Pressure
    (ATM)
    Catalog
    No.
    4.0 2.0 3 2.5 65 0.014 6 4.5 PDC400
    5.0 2.0 3 2.5 65 0.014 6 4.5 PDC401
    6.0 2.0 3 2.5 65 0.014 4 3.5 PDC402
    7.0 1.0 3 2.5 65 0.014 4 3.5 SO101
    7.0 2.0 3 2.5 65 0.014 4 3.5 PDC403
    8.0 1.0 3 2.5 65 0.014 4 3.5 SO102
    8.0 2.0 3 2.5 65 0.014 4 3.5 PDC404
    9.0 1.0 4 3.5 65 0.014 3.5 3 SO103
    9.0 2.0 4 3.5 65 0.014 3.5 3 PDC405
    9.0 4.0 4 3.5 65 0.014 3.5 3 PDC407
    10.0 1.0 4 3.5 65 0.014 3.5 3 SO104
    10.0 2.0 4 3.5 65 0.014 3.5 3 PDC406
    10.0 4.0 4 3.5 65 0.014 3.5 3 PDC408

    The devices listed have CE mark approval. Any customer or distributor outside of the EU will be subject to their individual country's regulations in regards to the importation and sale of these products.

    This publication could include technical or other inaccuracies or typographical errors. Changes are periodically added to the information herein; these changes will be incorporated in the new editions of the publication. NuMED Incorporated may make improvements and/or changes in the product(s) and/or the program(s) described in this publication at any time.