(Erba XL200) LACTATE DEHYDROGENASE-P, LDH 110, XSYS0013

NST ELAECCHC721

Valid Article

Former Code(s): ELAEZNL0606
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.
W01010120 - Lactate dehydrogenase p ( ldh - p --> l )
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.
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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(Erba XL200) REAGENT LACTATE DEHYDROGENASE-P, XSYS0013

Definition

Reagent for quantitative in vitro determination of LDH (DGKCH method) in human serum and plasma using an Erba XL chemistry automate..

Specifications

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Technical specifications

R1 and R2: Colourless liquids

Packaging & Labelling

R1: 2 x 44 ml - R2: 2 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.

Waste management

Mixture is not classified as hazardous. However, it contains a low concentration of toxic sodium azide with exposure limit. Please contact your watsan referent for advice on proper disposal.

Detailed hazard and precautionary information can be found in the safety data sheet (SDS).

MSF requirements

Use with the Erba XL200

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