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EUDAMED last updated this device on Jul 20, 2026
B-03760035441618STABILITY B is an MDD-legacy medical device registered in EUDAMED. It is classified as Class I. Manufactured by GROUPE SOBER SAS. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
03760035441618STABILITY B(01)03760035441618
European Medical Device Nomenclature — the EU product classification assigned to this device.
M030599IMMOBILISATION SYSTEMS AND DEVICES - OTHER3 warnings recorded — scroll inside the panel to see all entries.
Veillez à utiliser la bonne taille et la bonne référence. Ne pas laisser les sangles de réglage à la portée du patient. Surveiller le patient toutes les heures. Ne convient pas à des patients perturbés, désorientés & agités. Veiller à serrer les sangles modérément. Pose & utilisation uniquement sur prescription médicale. Garder hors de la portée des enfants. La supervision d’un adulte est recommandée.
Contre-indications : Ne pas utiliser ce produit pour des patients perturbés, désorientés, agités et/ou en sevrage (risque important de détérioration de la contention et risque important de chute du fauteuil ou d'étranglement pour le patient). Ne pas laisser les sangles de réglage et le système de fermeture à la portée du patient. Surveiller le patient toutes les heures (ne jamais le laisser sans surveillance).
La mise en place de ce produit est réalisée sous la responsabilité d’un professionnel de santé qualifié. Le praticien doit donner toutes les informations sur le produit au patient. Ce produit ne doit pas être en contact direct avec une plaie.
Primary placement in France; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Nov 10, 2016 | Still on market |
FR-MF-000017818Sterile
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.