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ARTERIAL ACCES SET, radial, 20Gx6cm, placement set, ster.

https://unicat.msf.org/cat/product/80468
STD SINSCACA2006S

Valid Article

The product is supplied (and stored) sterile, it must remain sterile until its use. Sterile = state of being free from all living microorganisms.
Single use
A single-use device, also referred to as a disposable device, is intended for use on one patient during a single procedure. It is not intended to be reprocessed (i.e., cleaned and disinfected or sterilized).
CE marking: declaration that the product meets EU standards for health, safety, and environmental protection. The CE marking indicates that the product may be sold freely in any part of the European Economic Area, regardless of its country of origin.
C0504 - Arterial introduction sets
European Medical Device Nomenclature (EMDN) is the nomenclature of use by manufacturers when registering their medical devices in the EUDAMED database. EMDN is characterised by its alphanumeric structure that is established in a seven-level hierarchical tree.
IIa
In Europe, medical material that fulfills the definition of a medical device according to the MDR (Medical Device Regulation) is classified into 4 classes
PM
The order of this product needs to be justified and is only acceptable under certain conditions.
CT3+
Thermosensitive codes are defined for storage and transportation temperature requirements of the products.
OC subscriptions: included in supply or field order tools (e.g. UniField)
SC subscriptions: included in supply or field tools
OC validations: approved for procurement and use by an OC for international or local orders specifying context and activity in Medical Standard Lists (MSL)
https://unicat.msf.org/web/image/product.template/587662/image_1920?unique=36bfefe

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CENTRAL ARTERIAL CATHETERIZATION SET

Definition

Catheter for arterial access intended for invasive blood pressure monitoring an obtaining blood samples for arterial blood gases analysis. The set contains also devices needed for the placement of the arterial catheter using the Seldinger technique.

Specifications

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Quality standards

EN ISO 10555-1, 2013, edition 3, +A1 2017 Sterile, single-use intravascular catheters - Part 1: General requirements

Technical specifications

  • Femoral set 5118.212
    • 1 arterial catheter 18 G - 12 cm Transparent PTFE (polytetrafluoroethylene) catheter tube, with 2 black O.R.X lines with a winged base to facilitate catheter attachment
    • 1 introducer needle 19G x 52 mm
    • 1 peelable application surface 100 x 150 cm
    • 10 non-woven compresses 7.5 x 7.5 cm
    • 1 catheter dressing 14 x 10 cm
    • 1 syringe 5 ml Luer Slip
    • 1 needle holder 14 cm
    • 1 scalpel N°11 short sleeve
    • 1 tray with 3 compartments 19 x 13 x 3 cm
  • Radial set 5118.906
    • ​1 arterial catheter ​20 G - 6 cm Transparent PTFE (polytetrafluoroethylene) catheter tube, with 2 black O.R.X lines with a winged base to facilitate catheter attachment
    • 1 introducer needle 20G x 35 mm
    • 1 peelable application field 50 x 97 cm 5.5 x 7.5 cm adhesive window
    • 10 non-woven compresses 7.5 x 7.5 cm
    • 1 catheter dressing 14 x 10 cm
    • 1 syringe 5 ml Luer Slip
    • 1 needle holder 14 cm
    • 1 scalpel N°11 short sleeve
    • 1 tray with 3 compartments 19 x 13 x 3 cm
  • Sterile, for single use

Packaging & Labelling

Sterile set in a tray peel open pack.

MSF requirements

Article needed for continuous invasive blood pressure monitoring for unstable intubated patients + easy blood sampling for repeated arterial blood gases analysis :

  • Mechanical ventilation for acute respiratory failure
  • And/or hemodynamic failure
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