ARROW PK-01451-WS One-Lumen PICC User Guide

ARROW PK-01451-WS One-Lumen PICC

Contents

• 1: One Lumen Catheter: 4 Fr. (1.45 mm OD) x 55 cm, T-Port Connector, Blue FlexTip®, Contamination Guard and Placement Wire
• 1: GlideThruTM 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: Catheter: 22 Ga. x 1-3/4″ (4.45 cm) Radiopaque over 25 Ga. RW Introducer Needle
• 1: Injection Needle: 18 Ga. x 1-1/2″ (3.81 cm)
• 1: Introducer Needle: 21 Ga. x 1-1/2″ (3.81 cm) TW
• 1: Introducer Needle: Echogenic 21 Ga. x 2-3/4″ (7 cm) TW
• 1: Syringe: 10 mL Luer-Slip
• 1: Skin Protectant Prep
• 1: 3 mL Applicator 2% CHG and 70% IPA ChloraPrep®1 One-Step Solution with Hi-Lite OrangeTM Tint
• 1: Dust Cap: Non-Vented
• 1: SecondSiteTM Adjustable Hub: Catheter Clamp
• 1: SecondSiteTM Adjustable Hub: Fastener
• 1: SharpsAway® Disposal Cup
• 1: Towel
• 1: Towel: 24″ x 36″ (61 cm x 91 cm)
• 1: Drape: 24″ x 36″ (61 cm x 91 cm) with 4″ (10 cm) fenestration
• 1: Forceps
• 1: Patient ID Card
• 1: Chart Sticker
• 1: Patient Information Booklet
• 1: Dressing: OpSite®2 14 cm x 10 cm
• 2: Paper Tape Measure 1: Tourniquet
• 5: Gauze Pad: 2″ x 2″ (5 cm x 5 cm)
• 6: Gauze Pad: 4″ x 4″ (10 cm x 10 cm)
• 1: Dressing: STATLOCK®3 Catheter Stabilization Device
• 2: Surgical Apparel: Mask
• 1: Surgical Tape: TransporeTM4 1″ x 54″ Roll
• 1A registered trademark of CareFusion or one of its subsidiaries.
• 2A registered trademark of T.J. Smith & Nephew, Limited.
• 3A registered trademark of C. R. Bard, Inc.
• 4A trademark of 3M Company.

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. www.P65Warnings.ca.gov
Not made with natural rubber latex.
Store between 15 ­ 30°C (59 ­ 86°F). Avoid freezing and excessive heat above 40°C (104°F). Fluid path components are non-pyrogenic.

Contraindications

The PICC is contraindicated wherever there is the presence of device-related infections or presence of thrombosis in the intended insertion vessel or catheter pathway. A 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 a maximum pump pressure of 10 PSIG and represent approximate flow capabilities

References

• Harm.P65Warnings.ca

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