Alanine Aminotransferase (ALT) Test Kit (IFCC)

Dénomination commerciale

Alanine Aminotransferase (ALT) Test Kit (IFCC)

Code d'IUD-ID

06971674862116

IUD-ID de base

B-06971674862116

Numéro de référence/catalogue

R1:100mL×1 R2:25mL×1(708)

Entité d'attribution

GS1

Catégorie de risque

IVDD — Général

Législation applicable

IVDD [Directive 98/79/CE relative aux dispositifs médicaux de diagnostic in vitro]

Statut

Sur le marché

Quantité

1

Description complémentaire du produit

For the in vitro quantitative determination of the activity of alanine aminotransferase (ALT) in human serum or plasma. Alanine aminotransferase (ALT), also known as glutamic-pyruvic transaminase (GPT), has a relatively high concentration in the liver, while its content is low in the kidneys, heart, skeletal muscles, pancreas, spleen, and lungs. Generally, the elevation of ALT is caused by certain liver-related diseases, including viral or toxic hepatitis and obstructive jaundice; ALT elevation is also seen in conditions such as extensive injury, muscle diseases, circulatory failure accompanied by shock and oxygen deficiency, myocardial infarction, and hemolytic diseases. The determination of alanine aminotransferase activity holds important value for the auxiliary diagnosis of the aforementioned diseases. This test is a preliminary screening method and does not have the effectiveness of diagnosing diseases. It needs to be comprehensively judged in conjunction with other test results.The main methods used for alanine aminotransferase detection in clinical practice include the alanine substrate method, as well as the alanine substrate-pyruvate oxidase method and the 2,4-dinitrophenylhydrazine method.

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.

• W01010103ALANINE AMINO-TRANSFERASE

Aucun certificat ne référence l'IUD-ID de base de ce dispositif.