48 tests/kit

Dénomination commerciale

non renseigné

06972221451173

B-06972221451173

Numéro de référence/catalogue

48 tests/kit

GS1

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

This kit is used for the in vitro qualitative detection of Ureaplasma urealyticum (UU) nucleic acid specifically in human urine samples, female cervical swabs, or male urethral swabs. The main target populations of this kit include patients with Ureaplasma urealyticum infection in the genital tract, people with a history of unsafe sexual contact or multiple sexual partners, people with a history of close contact with patients, and people with related clinical symptoms. This kit can be used for the differential diagnosis of urinary and genital tract related infections caused by Ureaplasma urealyticum pathogens. Ureaplasma urealyticum (UU), also known as Mycoplasma urealyticum, is a kind of prokaryotic microorganism between bacteria and viruses. Ureaplasma urealyticum is a common parasitic mycoplasma in the human urinary and genital tract. It is symbiotic with the human body and can cause disease when the internal environment changes or immunity decreases. It usually causes urinary tract infections and genital system infections. Clinically, the common manifestations are frequent urination, urgent urination, urine pain, increased urethral secretions and other symptoms, and serious cases may even cause salpingitis, ovaritis and other complications, which may lead to infertility. At present, the laboratory detection methods of Ureaplasma urealyticum infection mainly include: culture method, antigen detection method, real-time fluorescence PCR, etc. The test results of this kit serve as a valuable clinical reference but should not be used as the only criterion for clinical diagnosis. It is recommended to make a comprehensive analysis of the disease in combination with the patient's clinical manifestations and diagnostic methods.

URL des informations complémentaires

Aucune URL d'informations complémentaires renseignée par le fabricant.

Dimensions cliniques

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

• W0105011699BACTERIOLOGY - NA REAGENTS - OTHER