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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

VidaGesund — Class I MDR by VidaWell GmbH

MD Atlas
VidaWell GmbH

EUDAMED last updated this device on Apr 1, 2026

VidaGesund

426258496VidaGesundUU

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: VidaWell GmbH
UDI-DI code: 04262584960002
Reference / catalog number: VidaGesund

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Manufacturer information

Organization name: VidaWell GmbH
SRN: DE-MF-000052996
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	May 25, 2021	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04262584960002
Basic UDI-DI: 426258496VidaGesundUU
Reference / catalog number: VidaGesund
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: „VidaGesund“ dient dem medizinischen Selbstmanagement des Patienten in Form einer Therapiebegleitung für chronisch Kranke in Ergänzung einer ärztlich vorgenommenen wie begleiteten Diagnose und Therapie. Hierfür stellt die Anwendung dem Nutzer eine interaktive Gesundheitsakte zur Verfügung, in welcher dieser persönliche Daten sammeln, Ziele und Termine festlegen, Dokumente speichern, Notfallinformationen hinterlegen, Gesundheitstagebücher führen und Werte aus Laborberichten dokumentieren kann. Die im Rahmen der Gesundheitsakte hinterlegten Gesundheitsdaten werden von der Anwendung anhand medizinisch valider Datensätze ausgewertet und aufbereitet...
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V92MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

This device is not currently linked to any other device.

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.