- Low-profile adapter
- Lumen and French sizes on catheter
- Smooth-molded bifurcation
- Soft silicone atraumatic tip
- Comfortable finger grip
- Radiopaque silicone construction
{"AlternateComparison":false,"RelatedProducts":false,"Specification":true,"FeatureBenefit":false}
Central IV catheters
Hickman™ and Broviac™ Central Venous Catheters
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Hickman™ triple lumen catheter with peel-apart introducer
Support
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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
850 W Rio Salado Pkwy, Tempe, AZ 85281 United States
Customer Service
1.844.8.BD.LIFE (1.844.823.5433)
6:00 a.m. – 4:30 p.m. Arizona Time (Monday-Friday)
1.800.440.5376
- Overview
- Specifications
- eIFUs and Resources
- FAQ
- Product Notifications
true
FEATURE AND BENEFIT CARDS NOT AVAILABLE
FEATURE AND BENEFIT CARDS NOT AVAILABLE
false
*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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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 |
false
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false
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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
Recall Notifications
These recall notices provide current information on medical device recalls.
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false