EUYI β-Globin Gene Variation Test

Dénomination commerciale

EUYI β-Globin Gene Variation Test

06976457970057

B-06976457970057

Numéro de référence/catalogue

100THB-24

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: R24; Size: 24 Tests/kit. 2. The EUYI β-Globin Gene Variation Test can qualitatively detect the 619bp deletion in human β-globin gene in whole blood samples. Meantime, the PCR products of the assay also include the mutation region of β-globin gene which can be used for further analysis. The use of the test is indicated in: 1) Screening for the 619bp deletion of β-globin gene in suspicious populations. 2) Assisting the treatment and genetic counseling of hereditary hemolytic anemia diseases. 3. Stored at below -18℃. 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.

• W0106010111THALASSAEMIA

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.