ARROW EU-25541-IR Pressure Injectable One-Lumen PICC Instruction Manual

June 4, 2024
Arrow

ARROW EU-25541-IR Pressure Injectable One-Lumen PICC

ARROW-EU-25541-IR-Pressure-Injectable-One-Lumen-PICC-
PRODUCT

Contents

  • 1: One Lumen Catheter: 4 Fr. (1.45 mm OD) x 55 cm, Pressure Injectable, Blue FlexTip®
  • 1: GlideThru™ Peel-Away Sheath: 4 Fr. x 2-3/4″ (7 cm) Radiopaque over 4 Fr. Dilator
  • 1: Spring-Wire Guide: .018″ (0.46 mm) dia. x 13-1/8″ (33 cm) (Straight Soft Tip on Both Ends)
  • 1: Spring-Wire Guide, Marked: .018″ (0.46 mm) dia. x 51-3/16″ (130 cm) (Straight Soft Tip on One End – Straight Stiff Tip on Other)
  • 1: Introducer Needle: Echogenic 21 Ga. x 2-3/4″ (7 cm) TW
  • 1: Syringe: 10 mL Luer-Lock
  • 1: SecondSite™ Adjustable Hub: Catheter Clamp
  • 1: SecondSite™ Adjustable Hub: Fastener
  • 1: SharpsAway® II Locking Disposal Cup
  • 1: Catheter Trimmer
  • 1: Safety Scalpel: #11
  • 1: Patient ID Card
  • 1: Patient Information Booklet 1: Chart Sticker
  • 1: Paper Tape Measure
  • 1: Tourniquet
  • 1: Dressing: GRIP-LOK®1 Catheter Fixation Devic
  • 1: Valve: MicroCLAVE®2 Neutral Displacement Connector

1A registered trademark of TIDI. 2A registered trademark of ICU Medical, Inc. All components are CE 2797 unless otherwise noted.

Warning: Read all package insert warnings, precautions, and instructions prior to use. Failure to do so may result in severe patient injury or death. www.teleflex.com/IFU Not made with natural rubber latex. Fluid path components are non-pyrogenic.

Contraindications: The Pressure Injectable PICC is contraindicated wherever there is the presence of device-related infections or the presence of thrombosis in the intended insertion vessel or catheter pathway. Clinical assessment of the patient must be completed to ensure no contraindications exist.

ARROW-EU-25541-IR-Pressure-Injectable-One-Lumen-PICC-
FIG1

Priming volumes are approximate and are done without accessories. † Flow rate values are approximate and are determined using deionized water at 100 cm head height. †† Pump flow rates are determined at a maximum pump pressure of 10 psig and represent approximate flow capabilities. Pressure injection flow rates are determined at the injector pressure setting of 300 psi maximum using media of 11.8 centipoise viscosity, with 152 cm pressure tubing.

EU Authorized Representative and Importer:

Teleflex Medical IDA Business and Technology Park Dublin Road, Athlone Co. Westmeath, Ireland Arrow International LLC Subsidiary of Teleflex Incorporated 3015 Carrington Mill Blvd. Morrisville, NC 27560 USA LBL056795 R00 (2021-06)

References

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