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Organization name
UDI-DI code
Reference / catalog number

Kinetec Centura B&W — Class IIa MDR by Kinetec SAS

MD Atlas
Kinetec SAS

EUDAMED last updated this device on Mar 16, 2026

Kinetec Centura B&W

376024624SHOULDERCPMCG

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Kinetec SAS
UDI-DI code: 03760246246927
Reference / catalog number: 462100360X

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Manufacturer information

Organization name: Kinetec SAS
SRN: FR-MF-000000364
Manufacturer status: Active

Related devices

6080 avec chaise376024624ELBOWCPMUDOn the market 4621003102 376024624SHOULDERCPMCGOn the market Centura Lite376024624SHOULDERCPMCGOn the market Kinetec 6080376024624ELBOWCPMUDOn the market Kinetec 6080 avec module de coude376024624ELBOWCPMUDOn the market

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.

CW030
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Mar 3, 2006	Still on market

Device identification

Trade name: Kinetec Centura B&W
UDI-DI code: 03760246246927
Basic UDI-DI: 376024624SHOULDERCPMCG
Reference / catalog number: 462100360X
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Model with a mobile stand instead of a chair in order to allow the use of the device for patient in medical bed or in wheelchair
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z120603PASSIVE REHABILITATIVE GYMNASTICS EQUIPMENT

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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Expiration date
Manufacturing date
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Software identification