V2.1.0

Organization name

MoveUp

SRN

BE-MF-000011309

Manufacturer status

Active

1 warning recorded — scroll inside the panel to see all entries.

• CW011

  (Type)Caution-(Description)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[-]

Primary placement in Netherlands; available across 4 countries total.

Trade name

not provided

UDI-DI code

G166MOVEUP210MDRE6

Basic UDI-DI

++G166MOVEUP210MDRE6

Reference / catalog number

V2.1.0

Issuing entity

HIBCC

Risk category

Class IIa

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

—

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

• V92MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES

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Certificate health across this manufacturer's portfolio.