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EUDAMED last updated this device on Jun 30, 2026
B-03661379215425ArthroVims pump is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by HEMODIA SAS. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0366137921542510001433(01)03661379215425
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z1202110201MOTORISED ARTHROSCOPIC SURGERY SYSTEMS5 warnings recorded — scroll inside the panel to see all entries.
Le système peut être affecté par des interférences électromagnétiques générées par d’autres instruments. Vérifier que les autres instruments utilisés au bloc opératoire soient conformes à la norme IEC 60601-1-2 de compatibilité electromagnétique (CEM).
Pour éviter tout risque de choc électrique ne pas connecter le dispositif à une source d’alimentation non ou mal reliée à la terre. Risques d’électrocution : ne pas retirer le carter. Les réparations ne doivent être effectuées que par du personnel qualifié.
L’utilisation de la pompe «ArthroVims pump» est interdite lorsque l’arthroscopie est contreindiquée.
FR-MF-000007191 31618OTHER
Il est obligatoire de lire la notice avant une première utilisation de la pompe
Primary placement in France; available across 4 countries total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | — | Still on market |
| Belgium | — | Still on market |
| Hungary | — | Still on market |
| Poland | — | Still on market |
Sterile
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 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.No certificate specifically references this device's Basic UDI-DI.
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