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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

Kinetec SAS — Class IIa MDR by Kinetec SAS

MD Atlas
Kinetec SAS

EUDAMED last updated this device on Jan 22, 2026

Kinetec SAS

376024624KNEECPMGJ

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Kinetec SAS
UDI-DI code: 03760246246811
Reference / catalog number: 46210060X3

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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.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jan 1, 2003	Jan 22, 2026

Device identification

Trade name: Kinetec SAS
UDI-DI code: 03760246246811
Basic UDI-DI: 376024624KNEECPMGJ
Reference / catalog number: 46210060X3
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: Dispositif d'immobilisation passive pour le genou
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

Batch number
Expiration date
Manufacturing date
Serial number
Software identification