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BD 382269 - Catheter 14gx5-1/4" Angiocath IV 10/Bx, 5 BX/CA

BD  # 382269 - Catheter 14gx5-1/4
Part Number BD 382269
SKU Number CIA1119560
Sell Unit CASE
Ships Within 24 Hours
List Price $1,246.69
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Product Description

BD 382269 - Catheter 14gx5-1/4" Angiocath IV 10/Bx, 5 BX/CA

BD 382269 Angiocath IV Catheter

BD Angiocath Peripheral IV Catheters are designed for smooth insertion. They are made with FEP (Fluorinated Ethylene Propylene) polymer. FEP (Fluorinated Ethylene Propylene) polymer catheter material features a thin-wall design and a tapered tip that results in a smooth insertion and optimal flow rates.

  • Made of radiopaque FEP polymer
  • Thermo-moulded bevel ensures excellent penetration properties
  • Recommended for infusion, transfusion, angiography
  • Triple-bevel needle
  • Transparent clear flashback chamber
  • Available in longer lengths (14 G and 16 G available with 83 mm and 133 mm long catheters)
  • Diameters 12 G and 10 G permit very large volume emergency infusions
  • BD Luer-Lok compatible
  • Sterile, single use
  • Disposable to help reduce cross contamination
  • Available in longer lengths for special placement (3.00, 3.25, and 5.25 inches)

BD 382269 Angiocath IV Catheter Specifications

Catalog No.ColorGaugeCatheter Length (in)Catheter ID (mm)Catheter OD (mm)Gravity Flow Rate
382269Orange145.251.529 - 1.6462.088 - 2.12921910/Box 50/Case

What is Angiocath IV Catheter

A sterile, thin, flexible tube intended to be inserted into the peripheral vasculature of a patient to enable short-term (< 30 days) intravascular access; it is not intended to be advanced to the central vasculature. It typically includes dedicated accessories to facilitate catheter introduction/placement and function (e.g., connectors, injection ports, stylet and/or wings for fixation). It may be used for blood sampling, monitoring of blood pressure, to administer fluids, medication and/or for the injection of contrast media. This is a single-use device. AcessGUDID

BD 382269 Angiocath IV Catheter Device Characteristics

What MRI safety information does the labeling contain?MR Conditional
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):No
Device labeled as "Not made with natural rubber latex":No
For Single-Use:Yes
Prescription Use (Rx):Yes
Over the Counter (OTC):No
Combination Product:No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):No
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