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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

STABILIG CENTRO — Class I MDD by GROUPE SOBER SAS

MD Atlas
GROUPE SOBER SAS

EUDAMED last updated this device on Jun 23, 2025

STABILIG CENTRO

B-03701459804504

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: GROUPE SOBER SAS
UDI-DI code: 03701459804504
Reference / catalog number: STABILIG CENTRO

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Manufacturer information

Organization name: GROUPE SOBER SAS
SRN: FR-MF-000017818
Manufacturer status: Active

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Certificates

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.

Critical warnings

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

CW018
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 1 country total.

Placed on the market in France; per-country availability dates not published.

Device identification

Trade name: STABILIG CENTRO
UDI-DI code: 03701459804504
Basic UDI-DI: B-03701459804504
Reference / catalog number: STABILIG CENTRO
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Attelle de genou articulée réglable. Cadrans latéraux monocentriques permettant soit : - Une immobilisation de 0° à 90° (Réglage par amplitude de 10°). - Amplitude articulaire réglable entre deux butées (Flexion (30°, 40°, 70° & 90°) / Extension (0°, 10° & 30°)). - Une libération articulaire (butée anti-recurvatum). Fermeture facile par auto-agrippant.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: TU - H43

EMDN nomenclature code(s)

Y061209KNEE ORTHOSES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

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