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EUDAMED last updated this device on Feb 4, 2026
++G166MOVEUP200MDRDTmoveUP is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by MoveUp. Placed on the EU market in Belgium. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
G166MOVEUP200MDRDT2.2.0G166MOVEUP200MDRDT
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA / IFA support is coming.
European Medical Device Nomenclature — the EU product classification assigned to this device.
V92MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES1 warning recorded — scroll inside the panel to see all entries.
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. alert moveUP companion 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. alert 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 Belgium; available across 4 countries total.
| Country | On market since | Until |
|---|---|---|
| BelgiumPrimary placement | Jan 27, 2026 | Jan 27, 2028 |
| Germany | Jan 27, 2026 | Jan 27, 2028 |
| France | Jan 27, 2026 | Jan 27, 2028 |
| Netherlands | Jan 27, 2026 | Jan 27, 2028 |
BE-MF-000011309Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
View in glossary →Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
View in glossary →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →No certificate specifically references this device's Basic UDI-DI.
Certificate health across this manufacturer's portfolio.
20M00002SUP02SupplementedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →