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Long-term hemodialysis catheters Hickman™ Long-Term Hemodialysis Catheter

Hickman™ Dialysis/Apheresis 13.5 Fr Chronic Dual-Lumen Catheter kit, 36 cm overall Length, 19 cm Insertion Length

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1.844.8.BD.LIFE (1.844.823.5433)
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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
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Overview
  • Medical-grade radiopaque silicone
  • Excellent biocompatibility and visibility
  • Attachable suture wing
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Features and Benefits
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References

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

00801741037511

1

GTIN - Case

10801741037518

12


Quantity - Each

1


French Size

13.5

Total Length

36 cm

Insertion Length

19 cm

Tip to Hub Length

27 cm

GTIN

GTIN - each 00801741037511 1
GTIN - Case 10801741037518 12

Packaging

Quantity - Each 1

Product Basic Specification

French Size 13.5
Total Length 36 cm
Insertion Length 19 cm
Tip to Hub Length 27 cm
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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
Recall Notifications
These recall notices provide current information on medical device recalls.
Learn more
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