KA BAD - enlivio WebApp

Nom de l'organisation

room4 Softwareentwicklung GmbH

SRN

AT-MF-000004591

Statut du fabricant

Actif

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

• CW010

  enlivio enables therapists and physicians to provide teletherapeutic care to their patients and offer personalized exercise therapy at home. The enlivio software itself does not make any medical or therapeutic decisions. All medical or therapeutic decisions, as well as the decision to use enlivio for teletherapeutic care are made by the medical specialist, called “therapist” in the following (such as physiotherapists / physician / other occupational therapists in the field of medical-technical services). Important: The use of enlivio cannot replace a visit to a doctor or therapist. Patients with the following characteristics can be treated with enlivio: General: patients must be over 18 years of age. Medical Requirements: The use of enlivio is only suitable for patients who are eligible for medical exercise therapy. The decision for teletherapeutic care of patients is always up to the therapist. Enlivio is certified as a medical product for a) orthopedics and traumatology, b) neurology and c) internal medicine. It is important to note that for corresponding contraindications the use of enlivio is not permitted. Technical requirements: Patients must be in possession of an internet-enabled smartphone or tablet and be able to use it independently. Only devices with an Android operating system with version 5.0 or higher, or with an iOS operating system with version 12.0 or higher are supported. Regular updates of the software are mandatory in order to enable secure teletherapeutic training.

Marché principal en Autriche ; disponible dans 1 pays au total.

Commercialisé en Autriche ; dates par pays non publiées.

Dénomination commerciale

non renseigné

Code d'UDI-DI

09120143773041

Basic UDI-DI

912014377ENLIVIOBASEX2

Numéro de référence/catalogue

KA BAD - enlivio WebApp

Entité d'attribution

GS1

Catégorie de risque

Classe I

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.

• Z12069092VARIOUS PHYSIOTHERAPY AND REHABILITATION INSTRUMENTS - MEDICAL DEVICE SOFTWARE

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• Date d'expiration
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