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Central IV catheters Hickman™ and Broviac™ Central Venous Catheters

Hickman™ triple lumen catheter with peel-apart introducer

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1.844.8.BD.LIFE (1.844.823.5433)
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Ordering
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1.844.8.BD.LIFE (1.844.823.5433)
Onsite Visiting
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850 W Rio Salado Pkwy, Tempe, AZ 85281 United States
Customer Service
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1.844.8.BD.LIFE (1.844.823.5433)
6:00 a.m. – 4:30 p.m. Arizona Time (Monday-Friday)
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1.800.440.5376
Overview
  • Low-profile adapter
  • Lumen and French sizes on catheter
  • Smooth-molded bifurcation
  • Soft silicone atraumatic tip
  • Comfortable finger grip
  • Radiopaque silicone construction
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Features and Benefits
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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 - Each

00801741052019

1

GTIN - Case

10801741052016

12


Repair Kit

0601790 body, 0601690 red, 0601680 white, 0601730 blue

Quantity - Each

1


French Size

10 F

Total Length

97 cm

Volume

1.4 ml red, 0.8 ml white, 0.8 ml blue

Lumen Size

3.3 mm/1.5 mm red, 0.8 mm white, 0.8 mm blue

GTIN

GTIN - Each 00801741052019 1
GTIN - Case 10801741052016 12

Packaging

Repair Kit 0601790 body, 0601690 red, 0601680 white, 0601730 blue
Quantity - Each 1

Product Basic Specification

French Size 10 F
Total Length 97 cm
Volume 1.4 ml red, 0.8 ml white, 0.8 ml blue
Lumen Size 3.3 mm/1.5 mm red, 0.8 mm white, 0.8 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
false
Related Products
RELATED PRODUCTS NOT AVAILABLE
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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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