Luteinizing Hormone（LH）Detection Kit（Magnetic Solid Phase Chemiluminescent Immunoassay)

Dénomination commerciale

Luteinizing Hormone（LH）Detection Kit（Magnetic Solid Phase Chemiluminescent Immunoassay)

Code d'IUD-ID

06974969981073

IUD-ID de base

B-06974969981073

Numéro de référence/catalogue

50 Tests/kit（DR1026-1）

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

It is used for quantitative in vitro detection of luteinizing hormone (LH) in human serum. Luteinizing hormone is a glycoprotein consisting of α and β subunits, with a molecular weight of approximately 28.5 kilodaltons. Its α subunit has similarities with the α subunits of follicle-stimulating hormone (FSH), human chorionic gonadotropin (hCG), and thyroid-stimulating hormone (TSH), while the β subunit has unique biochemical properties and is crucial for its physiological functions. Luteinizing hormone plays an important role in endocrine regulation in the human body, mainly participating in the regulation of sexual gland functions: for men, it can regulate the synthesis and secretion of testosterone, maintaining normal physiological functions of the gonads; for women, it participates in the regulation of the basic functions of the gonads and maintaining the homeostasis of the endocrine system. Detecting the level of luteinizing hormone in serum can be used to assist in evaluating the function of the human endocrine system, screening the functional abnormalities of related endocrine glands such as the pituitary and gonads, providing reliable laboratory evidence for clinical diagnosis and monitoring of endocrine metabolic-related diseases, and helping clinicians diagnose and intervene in endocrine disorder-related diseases.

URL des informations complémentaires

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Dimensions cliniques

Aucune dimension clinique enregistrée pour ce dispositif.

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

• W0102050105LUTEINISING HORMONE

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