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BEDSIDE CONTROL CARD, ABO compatibility (Eldon)

https://unicat.msf.org/cat/product/19062
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Former Code(s): DDGTBLOG1CR
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.
W01030309 - Combined abo typing + rhesus typing
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.
S
The order of this product needs to be justified and is only acceptable under certain conditions.
CT30
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)

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BEDSIDE CONTROL CARD, ABO (Eldon)

Definition

Test performed "at the patient's bedside" immediately prior to transfusion to verify ABO compatibility between the recipient blood and the unit to be transfused.

Specifications

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Technical specifications

  • Double plastic-coated card (105 x 73 mm) with dessicated reagents
  • 4 reaction zones: 2 anti-A and 2 anti-B
  • Twin card; 1 donor side and 1 recipient side
  • Spots of dried monoclonal antibodies

Packaging & Labelling

Aluminium packaging per 25 cards

Packaging adhesive foils and mixing sticks: bag of 100 pieces.

To be Ordered Separately

  • Transparent adhesive foils: 2 per card (packaged by 100), ref. 2511/2551
  • Mixing sticks: 4 per card (packaged by 50)
  • 1 safety lancet per card
  • 1 ampoule of physiological saline solution

(see related articles below)

Instructions for use

The ultimate pretransfusional control card allows preventing ABO incompatibility accidents resulting from blood unit or patient misidentification.

The control must be performed at the patient's bedside immediately prior to transfusion by the nurse or the medical doctor who performs the transfusion.

The ABO group of the recipient is verified from a capillary blood sample, and the one of the blood unit from a tubing segment.

To perform the test you need a drop of water (distilled, filtered or water for injection).

This test is not a substitute for patient and donor ABO Rh D blood grouping or laboratory "cross-matching" test.

Keep the card in the patient's medical file after covering it with one transparent adhesive foil once it is dry.

Do not open the zipper of the Eldon bag below 18°C.

Eldon card that have been out if their bag for more than 30 minutes should be used that same working day.

Storage

  • Store between 5º and 37ºC
  • Shelf life: 2 years
  • Stable 6 months after firts opening. Ensure dessicanbt is present and that reagent sides face towards the label of the bag.
  • Guaranteed minimum remaining shelf life at delivery: 1/3 of the total shelf life
  • Not to be used beyond expiry date

(Cf Introduction: Thermosensitive products)

MSF requirements

Ultimate pretransfusional control is compulsory.

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