AL800001

Nom de l'organisation

Technogenetics S.p.A

SRN

IT-MF-000025331

Statut du fabricant

Actif

3 avertissements enregistrés — faire défiler le panneau pour tout voir.

• CW008

  Inappropriately handling samples may lead to biohazardous infection. Do not touch the sample, control liquid, calibrators, mixture and waste liquids directly with your hands. Wear gloves and lab coat, if necessary, goggles as well during operation. Please, refer to the Safety and Data Sheet for each type of products. In case your skin contacts the sample, control liquid or calibrator etc. please follow standard laboratory safety procedure and consult a doctor.
• CW273

  When the MAIN POWER is on, non-authorized personnel must not open the rear cover or side cover of the instrument. Spillage of reagent or sample on the analyzer may cause equipment failure and even electric shock. Do not place sample and reagent or other liquids on the analyzer. In case of spillage, switch off the power immediately, remove the spillage and contact Customer Service Department of Technogenetics. When two switches in the left side of this equipment are off, inside power cables still connect with outside power. Only after switching off MAIN POWER, the risk of electric shock from AC power will not be exist
• CW011

  When the system is running, any part of the body, clothing or hair must be kept away from moving parts.

Marché principal en Italie ; disponible dans 1 pays au total.

Commercialisé en Italie ; dates par pays non publiées.

Dénomination commerciale

non renseigné

Code d'UDI-DI

08054320951032

Basic UDI-DI

805432095AL1200ANALYZER72

Numéro de référence/catalogue

AL800001

Entité d'attribution

GS1

Catégorie de risque

IVDR Classe A

Législation applicable

IVDR [Règlement (UE) 2017/746 relatif aux dispositifs médicaux de diagnostic in vitro]

Statut

Sur le marché

Quantité

1

Description complémentaire du produit

The AL1200 is an automated chemiluminescence analyzer for in vitro assays in clinical biology and autoimmunity that performs the sample processing (sample pre-dilution, sample and reagent dispensing, incubation, washing procedure), as well as measurement and interpretation of results

URL des informations complémentaires

Aucune URL d'informations complémentaires renseignée par le fabricant.

Dimensions cliniques

Aucune dimension clinique enregistrée pour ce dispositif.

Nomenclature européenne des dispositifs médicaux — la classification produit UE attribuée à ce dispositif.

• W0201020102AUTOMATED IMMUNOCHEMISTRY ANALYSERS - MODERATE ROUTINE (Throughput > 100 and <= 250 test/h)