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Ultraverse™ Ultraverse™ 018 PTA Dilatation Catheters

Ultraverse™ 018 PTA Dilatation Catheter, 7 mm x 120 mm balloon with 200 cm catheter

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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)
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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
  • Innovative, reinforced inner lumen promotes axial strength for crossing tight lesions
  • The GeoAlign™ Marking System is designed to help reduce radiation exposure by minimizing fluoroscopy time during repeat catheter placement*
  • Multiple catheter lengths available designed to enable access from alternative sites
  • For balloon lengths of 100 mm and greater, dual radiopaque markers are positioned on the distal portion of the balloon to differentiate the proximal and distal ends
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References

* The GeoAlign™ Marking System is not a replacement for fluoroscopy. When the catheter is exposed to the vascular system, the location of the balloon should be confirmed while under high quality fluoroscopic observation.

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

00801741156977

1


Quantity - Each

1


Balloon Diameter

7 mm

Balloon Length

12 cm

Catheter Length

200 cm

Sheath Size

5 F

GTIN

GTIN - each 00801741156977 1

Packaging

Quantity - Each 1

Product Basic Specification

Balloon Diameter 7 mm
Balloon Length 12 cm
Catheter Length 200 cm
Sheath Size 5 F
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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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