Ammonia (AMM) Test Kit (Glutamate Dehydrogenase)

Dénomination commerciale

Ammonia (AMM) Test Kit (Glutamate Dehydrogenase)

Code d'IUD-ID

06971674866343

IUD-ID de base

B-06971674866343

Numéro de référence/catalogue

R1a:25mL×1 R1b:5mL×1 R2:5mL×1（702）

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 detection of ammonia (AMM) content in human serum. The ammonia detection kit is used for the quantitative determination of ammonia content in human serum. Due to oxidative deamination, as well as diet and transamination of amino acids, the ammonia content in the normal human blood circulation is very low. The liver is the main organ involved in ammonia removal. A common clinical indicator of nervous system damage is an increase in blood ammonia concentration. 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 method used for ammonia detection in clinical practice is the glutamate dehydrogenase 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.

• W01010301AMMONIA

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