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Central IV catheters Broviac®, Hickman® and Leonard® central venous catheters

Hickman™ triple lumen catheter with peel-apart introducer

Overview
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Features and Benefits
Promotional Story
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References

*Not all product codes are offered in all regions.

Please consult Instructions for Use for product indications for use, contraindications, warnings, precautions, complications, adverse events and detailed safety information.

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Specification

GTIN - Case

10801741051972

12

GTIN - each

00801741051975

1


Repair Kit

0601740 body, 0601690 red, 0601680 white, 0601730 blue

Quantity - Each

1


French Size

12.5 F

Total Length

90 cm

Volume

1.6 ml red, 0.7 ml white, 0.7 ml blue

Lumen Size

4.1 mm/1.5 mm red, 1.0 mm white, 1.0 mm blue

GTIN

GTIN - Case 10801741051972 12
GTIN - each 00801741051975 1

Packaging

Repair Kit 0601740 body, 0601690 red, 0601680 white, 0601730 blue
Quantity - Each 1

Product Basic Specification

French Size 12.5 F
Total Length 90 cm
Volume 1.6 ml red, 0.7 ml white, 0.7 ml blue
Lumen Size 4.1 mm/1.5 mm red, 1.0 mm white, 1.0 mm blue
References
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Electronic Instructions for Use (eIFUs)
Resources
References
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Frequently Asked Questions
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References
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Related Products
RELATED PRODUCTS NOT AVAILABLE
References
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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.
Learn more
References
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