EUYI HPV Genotyping Kit Plus

Dénomination commerciale

EUYI HPV Genotyping Kit Plus

06976457970941

B-06976457970941

Numéro de référence/catalogue

100HPP-25

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

1. Type: R25, Spec: 25 tests/kit, 2 kits/set. 2. This kit is an in-vitro diagnostic test. The test is the qualitative and genotyping detection of DNA for 40 Human Papillomavirus (HPV) types in cervical specimens. Detected HPVs include 15 high-risk HPV (HR HPV), 6 possibly carcinogenic HPV and 19 low-risk HPV (LR HPV). High-risk HPV types: 16，18，31，33，35，39，45，51，52， 56，58，59， 68，73 and 82； Possibly carcinogenic HPV types: 26, 53, 66, 67, 69 and 70 Low-risk HPV types: 6 , 11, 30, 32, 34, 40, 42, 43, 44, 54, 55, 61, 62, 74, 81, 83, 84, 87 and 90. 3. Kit I should be stored below -18℃; Kit II at 2~8℃.. 4. In vitro diagnostic reagent for professional use only. 5. Intended solely for in vitro diagnostic purposes and not for therapeutic use.

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.

• W0105041004FULL GENOTYPING HIGH-RISK + LOW-RISK HPV - NA REAGENTS

1 avertissement enregistré — faire défiler le panneau pour tout voir.

• CW999

  For professional in vitro diagnostic use only. Handle all specimens as potential biohazard materials. Wear protective gloves and lab coat during operation. Keep out of reach of children. Dispose of waste according to local biomedical waste regulations.