(Erba XL200) REAGENT KIT UREA XSYS0020

STD ELAECCHC718

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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.
W01010204 - Urea/blood urea nitrogen
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.
Thermosensitive codes are defined for storage and transportation temperature requirements of the products.
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(Erba XL200) REAGENT KIT UREA , XSYS0020

Definition

Reagent for quantitative in vitro determination of urea (Urease GLDH method) in human serum, plasma et urine using an Erba XL chemistry automate.

Specifications

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Components

  • R1: 5 vials (44 ml)
  • R2: 5 vials (11 ml)

Technical specifications

  • R1 : Clear colourless liquid
  • R2: liquid
  • 1250 tests

Packaging & Labelling

R1: 5 x 44 ml - R2: 5 x 11 ml

To be Ordered Separately

  • Quality controls
  • Calibrators

Instructions for use

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Storage

  • The unopened reagents are stable till the expiry date stated on the bottle and kit label when stored at 2–8°C.
  • On board stability: minimum 30 days if refrigerated (2–10°C) and not contaminated.

MSF requirements

Use with the Erba XL200

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