ARROW PR-35552-HPHNM Pressure Injectable Two-Lumen PICC with 80 cm Wire Instructions
- June 4, 2024
- Arrow
Table of Contents
ARROW® PR-35552-HPHNM Pressure Injectable Two-Lumen PICC with 80 cm Wire
Instructions
5 Fr. 2 Lumen 55 cm catheter length .018 inch dia. spring-wire guide
Contents
1: Two Lumen TaperFree® Catheter: 5 Fr. (1.81 mm OD) x 55 cm, Pressure
Injectable, Blue FlexTip® and Contamination Guard
1: GlideThru™ Peel-Away Sheath: 5 Fr. x 4″ (10 cm) Radiopaque over 5 Fr.
Dilator
1: Spring-Wire Guide, Nitinol, Marked: .018″ (0.46 mm) dia. x 17-3/4″ (45 cm)
(Straight Soft Tip on One End – Straight Stiff Tip on Other)
1: Guidewire, Marked: .018″ (0.46 mm) dia. x 80 cm Hydrophilic-Coated Nitinol
with Soft Tip Tungsten Coil (CE 0120)
1: Introducer Needle: Echogenic 21 Ga. x 2-3/4″ (7 cm) TW
1: Syringe: 10 mL Luer-Lock
2: Dust Cap: Non-Vented
1: SecondSite™ Adjustable Hub: Fastener
1: SecondSite™ Adjustable Hub: Catheter Clamp
1: Catheter Trimmer 1: Safety Scalpel: #11
1: Patient ID Card
1: Chart Sticker
1: Patient Information Booklet
1: Checklist/CLIP Sheet
1: Paper Tape Measure
1: Dressing: STATLOCK®1 PICC Plus Catheter Stabilization Device
1A registered trademark of C. R. Bard, Inc.
All components are CE 2797 unless otherwise noted.
Rx only
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
California Prop. 65
WARNING: Cancer and Reproductive Harm.
Not made with natural rubber latex.
Fluid path components are non-pyrogenic.
Contraindications: The Pressure Injectable PICC is contraindicated wherever there is presence of device related infections or presence of thrombosis in the intended insertion vessel or catheter pathway. Clinical assessment of the patient must be completed to ensure no contraindications exist.
- 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 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
LBL062737 R00 (2021-11)