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Urological guidewires SOLO™ Hydro Hybrid Guidewire with Hydrophilic Coating

Guidewires, SOLO™ Hydro, Triton™ Core, Hydrophilic Coated Shaft and Straight Tip

Does not contain natural latex.

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1.844.8.BD.LIFE (1.844.823.5433)
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Ordering
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1.770.784.6100
bardmedical.customerservice@crbard.com
Onsite Visiting
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8195 Industrial Boulevard Covington, Georgia 30014 United States
Customer Service
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1.844.8.BD.LIFE (1.844.823.5433)
bardmedical.customerservice@crbard.com
Overview

The Solo™ Hydro Hybrid Guidewire is designed to facilitate the placement of diagnostic devices, therapeutic devices, and catheters. The guidewire is offered in a variety of diameters, tip designs, and stiffnesses. The Solo™ Hydro Hybrid Guidewire has a 5cm(1.96") hydrophilic coated polymer tip to facilitate access. The hydrophilic coating on the entire length of the wire aids in the trackability of devices. The guidewire comes in a protective hoop, sterile and ready for single use.

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Specification

GTIN - Pouch

00816840020197

1

GTIN - Box

10816840020194

5


Quantity

5/box


Size

Length 150cm, Wire Size 0.035"

GTIN

GTIN - Pouch 00816840020197 1
GTIN - Box 10816840020194 5

Packaging

Quantity 5/box

Product Basic Specification

Size Length 150cm, Wire Size 0.035"
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Product Complaints
North American Regional Complaint Center
1-844-8BD-LIFE (1-844-823-5433)
Things to Consider

If you are a patient or end user, you can contact us yourself, or you may have your caregiver or your physician do that for you. To help us process your
information quickly and effectively, please contact our customer complaints
team.

To better facilitate our investigation, please include the following information in your reporting:


  • Product Name and/or Catalog Number
  • Lot Number or Serial Number
  • Any injuries and/or Harm?
  • What is the issue you experienced?
  • Is the actual sample or sample representative available? (If possible, please send affected sample)
  • Contact name and phone number
Product Recalls
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Recall Notifications
These recall notices provide current information on medical device recalls.
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