ProtekDilate Vascular Access Kit

By integrating high‑quality materials with a layout optimized for ease of use, ProtekDilate was designed to elevate both the user experience and procedural workflow. The result is a kit that feels deliberate, intuitive, and aligned with the standards physicians expect in advanced clinical tools.
Four unique configurations

ProtekDilate is available in jugular, femoral, femoral super stiff, and dilator set

ProtekDilate Jugular Kit

The 12-piece ProtekDilate Jugular Kit is compatible with the ProtekDuo+™ Dual-Lumen Cannula. Order number is #5130-0830. Contents are:

  1. Guidewire, 0.035”, 180 cm
  2. 10 cc Syringe
  3. 18 Ga Echogenic Introducer Needle
  4. #11 Scalpel
  5. Sterilized Procedure Tray (pictured above)
  6. 8/10 Fr Dilator
  7. 14 Fr Dilator
  8. 18 Fr Dilator
  9. 22 Fr Dilator
  10. 26 Fr Dilator
  11. 28 Fr Dilator
  12. 30 Fr Dilator

ProtekDilate Femoral Kit

The 11-piece ProtekDilate Femoral Kit's order number is #5130-3801. Contents are:

  1. Guidewire with depth markers 0.038”, 180 cm
  2. 10 cc Syringe
  3. 18 Ga Echogenic Introducer Needle
  4. #11 Scalpel
  5. Sterilized Carrying Tray
  6. 8/10 Fr Dilator
  7. 14 Fr Dilator
  8. 16 Fr Dilator
  9. 18 Fr Dilator
  10. 22 Fr Dilator
  11. 26 Fr Dilator

Femoral Super Stiff

The 11-piece ProtekDilate Femoral Super Stiff kit's order number is #5130-0826. Contents are:

  1. Guidewire, 0.035”, 180 cm
  2. 10 cc Syringe
  3. 18 Ga Echogenic Introducer Needle
  4. #11 Scalpel
  5. Sterilized Carrying Tray
  6. 8/10 Fr Dilator
  7. 14 Fr Dilator
  8. 16 Fr Dilator
  9. 18 Fr Dilator
  10. 22 Fr Dilator
  11. 26 Fr Dilator

Dilator Set

The 11-piece ProtekDilate Dilator Set's order number is #5130-0007. Contents are:

  1. 10 cc Syringe
  2. 18 Ga Echogenic Introducer Needle
  3. #11 Scalpel
  4. Sterilized Carrying Tray
  5. 8/10 Fr Dilator
  6. 14 Fr Dilator
  7. 16 Fr Dilator
  8. 18 Fr Dilator
  9. 22 Fr Dilator
  10. 26 Fr Dilator
  11. 30 Fr Dilator

ProtekDilate Vascular Access Kit Comparison

(All sets have an 18 gauge Echogenic Introducer Needle, 10 cc Syringe, and #11 Scalpel)


 Jugular Femoral Femoral Super Stiff Dilator Set
Product Code 5130-0830 5130-3801 5130-0826 5130-0007
Guidewire 0.035”, 180cm

Guidewire with depth markers, 0.038”, 180cm

 0.035”, 180cm No wire
Dilator Sizes

8/10 Fr, 14 Fr, 18 Fr, 22 Fr, 26, Fr, 28 Fr, 30 Fr

8/10 Fr, 14 Fr, 16 Fr, 18 Fr, 22, Fr, 26 Fr

8/10 Fr, 14 Fr, 16 Fr, 18 Fr, 22, Fr, 26 Fr

8/10 Fr, 14 Fr, 16 Fr, 18 Fr, 22 Fr, 26, Fr, 30 Fr



ProtekDilate Vascular Access Kit Important Safety Information
  1. Indications for Use

The ProtekDilate Vascular Access Kits are intended for single use by a trained physician to assist in vessel cannulation.

  1. Contraindications for Use 

The guidewire is contraindicated for use in the coronary or cerebral vasculature. The physician is responsible to determine any patient conditions which may prohibit the safe use of the dilator sets. Use only as indicated.

  1. Warnings & Precautions

Assure that the vessel is of adequate size to accommodate the dilators being used. Avoid kinking dilators. DO NOT over dilate to a size larger than the intended use cannula. Over dilation may cause excessive bleeding. ALWAYS dilate vessels using dilators in order from smallest to largest. 

The device must be used in accordance with the instructions for use provided in the Instructions for Use. For a complete listing of warnings and precautions please refer to the Instructions for Use which accompany each product. Federal law (U.S.A.) restricts this device to sale by or on the order of a physician.

  1. Adverse Events

Potential adverse effects that may be associated with Venous Dilation include the following: Perforation or laceration of the venous wall; Thrombus formation; Vascular injury with or without the need for surgical intervention; Blood loss requiring fluid replacement or transfusion of blood products; Infection; Allergy or anaphylactic reaction to device.

The information contained in this summary represents partial excerpts taken from the product labeling. The information is not intended to serve as a substitute for a complete and thorough understanding of the device nor does this information represent full disclosure of all pertinent information concerning the use of this product. 

Please request the instructions for use containing full prescribing information including indications, contraindications, warnings, precautions and adverse events via the ‘Contact Us’ form on our website (www.livanova.com/cannulae). 

Legal Manufacturer:
Sorin Group Italia S.r.l.
Via Statale 12 Nord, 86
41037 Mirandola (MO) Italy
Tel: +39 0535 29811

Distributed in the US by:
LivaNova USA Inc.
14401 West 65th Way,
Arvada CO 80004
United States
Tel: (303) 425-5508, (800) 221-7943
www.livanova.com

© 2026 LivaNova PLC. All Rights Reserved.

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