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Teleflex RA-04020 - Radial Artery Catheterization Set, 20 GA X 1-3/4", 50/CS

Teleflex # RA-04020 - Radial Artery Catheterization Set, 20 GA X 1-3/4
Part Number Teleflex RA-04020
SKU Number CIA2043183
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List Price $1,412.22
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Product Description

Teleflex RA-04020 - Radial Artery Catheterization Set, 20 GA X 1-3/4", 50/CS

Teleflex RA-04020 Radial Artery Catheterization Set

The Arrow Arterial Catheterization Device permits access to the peripheral arterial circulation or to other small vessels.

  • 1 Catheter: 20 Ga. x 4.45 cm Radiopaque Polyurethane over 22 Ga. TW Introducer Needle with Integral .018" (0.46 mm) dia. Spring-Wire Guide
  • 1 Wing Clip: Suture

Teleflex RA-04020 Radial Artery Catheterization Set Precautions

  • Do not alter the catheter, guidewire, or any other kit/set component during insertion, use or removal.
  • Procedure must be performed by trained personnel well versed in anatomical landmarks, safe technique, and potential complications.
  • Some disinfectants used at catheter insertion site contain solvents which can weaken the catheter material. Alcohol, acetone, and polyethylene glycol can weaken the structure of polyurethane materials. These agents may also weaken the adhesive bond between catheter stabilization device and skin.
    • Do not use acetone or acetone-alcohol on or near the catheter surface.
    • Do not use alcohol to soak catheter surface or allow alcohol to dwell in a catheter lumen to restore catheter patency or as an infection prevention measure.
    • Do not use polyethylene glycol containing ointments at insertion site.
    • Allow insertion site to dry completely prior to applying dressing.
  • Indwelling catheter should be routinely inspected for desired patency, security of dressing, and possible migration.
  • Use standard precautions and follow established institutional policies and procedures.

Device Characteristics of Teleflex RA-04020 Radial Artery Catheterization Set

What MRI safety information does the labeling contain?Labeling does not contain MRI Safety Information
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":Yes
For Single-Use:Yes
Prescription Use (Rx):Yes
Over the Counter (OTC):No
Kit:Yes
Combination Product:No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):No
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