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MYCOBACTERIAL DETECTION SYSTEM (BACTEC MGIT 960)

https://unicat.msf.org/cat/product/13423
STD ELAEMDSE1--

Valid Article

Former Code(s): ELAEMGIT1-- ELAEMGIE1--
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.
W02030299 - Instruments for blood cultures and mycobacteria - other
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.
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The order of this product needs to be justified and is only acceptable under certain conditions.
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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MYCOBACTERIAL DETECTION SYSTEM BACTEC MGIT 960

Reserved for TB culture programmes.

Definition

Automated system for high-volume mycobacteria growth, detection and susceptibility testing. The instrument has a maximum capacity of 960 BBLTM MGITTM tubes (7ml).

Specifications

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Technical specifications

  • Fully automated
  • Capacity: 960 tubes
  • Mycobacteria detection and susceptibility testing

Dimensions

  • 134.6x 91.4 x 71.1 cm

Instructions for use

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Precautions for Use

Secure all biomedical electrical devices in the laboratory. Contact your biomedical referent to define the best option.

Failing that, use a UPS double conversion for the electrical protection of the apparatus (see related articles below).

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