Instruction Manual
EU-24052-HPMSB Pressure Injectable Two-Lumen PICC
Pressure Injectable Two-Lumen PICC
Contents:
1:TwoLumenCatheter:5Fr.(1.81mmOD)x40cm,PressureInjectable,T-PortConnector,BlueFlexTip®,ContaminationGuardandPlacementWire
1:GlideThru™Peel-AwaySheath:5Fr.x2-3/4″(7cm)Radiopaqueover5Fr.Dilator
1:Spring-WireGuide,Nitinol,Marked:.018″(0.46mm)dia.x17-3/4″(45cm)(StraightSoftTiponOneEnd-StraightStiffTiponOther)withArrowAdvancer
1:InjectionNeedle:Eclipse™122Ga.x1-5/8″(4cm)
1:InjectionNeedle:Eclipse™125Ga.x1″(2.54cm)RW
1:IntroducerNeedle:Echogenic21Ga.x2-3/4″(7cm)TW
1:FilterNeedle:18Ga.TWx1-1/2″(3.81cm)withBluntFillTip2:Syringe:10mLLuer-Lock
1:Syringe:3mLLuer-Lock
1:SecondSite™AdjustableHub:Fastener
1:SecondSite™AdjustableHub:CatheterClamp
1:SharpsAway®DisposalCup
1:SharpsAway®IILockingDisposalCup
1:CatheterTrimmer
1:Towel:24″x36″(61cmx91cm)
1:Drape:60″x76″(152cmx193cm)1:Drape:36″x41″(91cmx104cm)with3″x5″(8cmx13cm)fenestration
1:Towel
1:SafetyScalpel:#111:PatientIDCard1:SterileProcedureSign
1:PatientInformationBooklet1:ChartSticker
1:PICCLineInsertionChecklist
1:PaperTapeMeasure
1:Tourniquet5:GauzePad:2″x2″(5cmx5cm)
1:Dressing:Tegaderm®2I.V.4″x6″(10cmx15.5cm)
1:Dressing:GRIP-LOK®3CatheterFixationDevice10:GauzePad:4″x4″(10cmx10cm)
1:SurgicalApparel:Cap1:SurgicalApparel: ImperviousGown
1:Dressing:Steri-Strip®21/2″x4″(1.2cmx10cm)1:SurgicalApparel:Mask
1:SurgicalApparel: MaskwithShield
1:TransducerCover:4-12/16″x95″(12cmx244cm)2:Valve:MicroCLAVE®4NeutralDisplacementConnector
1:HemoHopper®FluidReceptacle1AtrademarkofBecton,DickinsonandCompany.
2Aregisteredtrademarkof3MCompany.
3AregisteredtrademarkofTIDI.
4AregisteredtrademarkofICUMedical,Inc.
AllcomponentsareCE2797unlessotherwisenoted.
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. A clinical assessment of the patient must be completed to ensure no contraindications exist.
 Lumen | Priming Volume* (mL) | Gravity Flow Rate† (mL/hr) | Pump Flow Rate†† (mL/hr) | MAX Pressure Injection Flow Rate** (mL/sec) |
| Distal ( 18 G a .) Proximal ( 18 G a.) | 0.36 0.38 | 416 475 | 3500 4090 | 4 4 |
* 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
2797Technology Park
Dublin Road, Athlone
Co. Westmeath, Ireland
Arrow International LLC
A subsidiary of Teleflex Incorporated
3015 Carrington Mill Blvd.
Morrisville, NC 27560 USA
www.teleflex.com
LBL056501 R 00 (2021-06)
noted.eu is available for purchase - Sedo.com
