moveUP MDR

Nom de l'organisation

MoveUp

SRN

BE-MF-000011309

Statut du fabricant

Actif

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

• CW011

  moveUP is not an emergency tool. In case of emergency please contact your doctor or call 112.moveUP is not intended to monitor/treat vital parameters of critical illness.moveUP is not a replacement for any treatment you need to follow, but is used as an addition.Patients need to be aware that if questionnaires are not completed on a frequent basis or not answered truthfully, the care team has more difficulty understanding your health situation & progress.The moveUP App offers personalized healthcare based on the patient’s profile and therefore can not be shared, borrowed or traded between users. The information and advice of the moveUP application do not apply to a patient other than the one whose profile is stored in the application.The patient may not grant access to the moveUP App to third parties. Any other person can, even accidentally, send wrong information or change the profile of the patient, with the result that the moveUP-guided advice no longer corresponds to the needs of the patient.The platform includes modules displaying wellness data. These data are not part of the medical device and are not intended to be used for clinical decision making

Marché principal en Belgique ; disponible dans 4 pays au total.

Dénomination commerciale

moveUP MDR

Code d'UDI-DI

G166MOVEUPV200AU

Basic UDI-DI

++G166MOVEUPV200AU

Numéro de référence/catalogue

2.0.0 MDR

Entité d'attribution

HIBCC

Catégorie de risque

Classe IIa

Législation applicable

MDR [Règlement (UE) 2017/745 relatif aux dispositifs médicaux]

Statut

Sur le marché

Quantité

1

Description complémentaire du produit

—

URL des informations complémentaires

Aucune URL d'informations complémentaires renseignée par le fabricant.

Dimensions cliniques

Aucune dimension clinique enregistrée pour ce dispositif.

• V92MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES

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