- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Apr 16, 2025
42700036055APP1E3memodio vida is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by memodio GmbH. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
042700036055191(01)04270003605519
European Medical Device Nomenclature — the EU product classification assigned to this device.
V92MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES2 warnings recorded — scroll inside the panel to see all entries.
Absolute Contraindications: Dizziness and giddiness (R42). Relative contraindications at the physician's discretion: Chronic or acute illness in which movement is contraindicated, in particular acute infections or fever, advanced heart disease, cancer and injuries (especially to the spine, hips and knees), injury, illness or medication-related sensory impairment (vision/hearing/balance/surface/depth sensitivity) that cannot be compensated for by aids or devices.
memodio does not replace a doctor or therapist. Any change in existing medications and/or treatments should not be made without consulting the treating physician. Contact your doctor in case of acute cognitive changes. If you suffer from pre-existing food intolerances or allergies, always check whether the dietary recommendations or recipe suggestions suggested in the memodio app contain ingredients that may trigger intolerances or allergic reactions in you. If this is the case, you should not implement these recommendations or recipes. Follow the instructions of your doctor regarding the exercises and movements you are allowed to perform in your particular health condition. The instructions always take precedence over the instructions in the app and must always be followed exactly. followed. Failure to follow your doctor's instructions when using memodio may result in pain and injury.
Primary placement in Spain; available across 1 country total.
Placed on the market in Spain; per-country availability dates not published.
DE-MF-000033704Sterile
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.
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.