PR-45041-BAS Pressure Injectable Arrowg+ard Blue Advance One-Lumen PICC Instruction Manual

: June 3, 2024
: Arrow

Table of Contents

Contents:
Rx only
References
Read User Manual Online (PDF format)
Download This Manual (PDF format)

Pressure Injectable Arrowg + ard Blue Advance® One-Lumen PICC

1: One Lumen Taper Free® Catheter with Arrowgard Blue Advance® Antimicrobial/Anti thrombogenic
Protection1: 4.5 Fr. (1.58 mm OD) x 50 cm, Pressure Injectable, T-Port Connector, Blue Flex Tip® and Placement Wire
1: Glide Thru™ Peel-Away Sheath: 4.5 Fr. x 2-3/4″ (7 cm) Radiopaque over 4.5 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: Safety Introducer Needle: Echogenic 21 Ga. x 2-3/4″ (7 cm) TW
1: Introducer Needle: Echogenic 21 Ga. x 2-3/4″ (7 cm) TW
1: Syringe: 10 mL Luer-Lock 1: Dust Cap: Non-Vented
1: Second Site™ Adjustable Hub: Catheter Clamp
1: SecondSiteTM Adjustable Hub: Fastener
1: SharpsAway® Disposal Cup
1: SharpsAway® II Locking Disposal Cup
1: Catheter Trimmer 1: Safety Scalpel: #11
1: Patient ID Card 1: Patient Information Booklet
2: Paper Tape Measure 1: Tourniquet
1: Dressing: STATLOCK®2 Catheter Stabilization Device 1Licensed under US Patent No. 7,329,412.
2A 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. www.P65Warnings.ca.gov

Not made with natural rubber latex.
Store below 25°C (77°F). Avoid excessive heat above 30°C (86°F).
Fluid path components are non-pyrogenic.

Contraindications: The Pressure Injectable Arrowgard Blue Advance antimicrobial/anti thrombogenic catheter is contraindicated:

for patients with known hypersensitivity to chlorhexidine
in the presence of device related infection in the intended insertion vessel or catheter pathway
in the presence of thrombosis in the intended insertion vessel or catheter pathway

Lumen| *Priming Volume (mL)| Gravity Flow
Rate† (mL/hr)| Pump Flow Rate††
(mL/hr)| MAX Pressure Injection Flow
Rate (mL/sec)
---|---|---|---|---
| | | |

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

LBL061089 R01 (2021-08)