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Organization name
UDI-DI code
Reference / catalog number

Optima Essential - KINETEC SAS — Class IIa MDR by Kinetec SAS

MD Atlas
Kinetec SAS

EUDAMED last updated this device on Mar 17, 2026

Optima Essential - KINETEC SAS

376024624KNEECPMGJ

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Kinetec SAS
UDI-DI code: 03760246246828
Reference / catalog number: 46210062X3

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Manufacturer information

Organization name: Kinetec SAS
SRN: FR-MF-000000364
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.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Feb 1, 2010	Still on market

Device identification

Trade name: Optima Essential - KINETEC SAS
UDI-DI code: 03760246246828
Basic UDI-DI: 376024624KNEECPMGJ
Reference / catalog number: 46210062X3
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: Passive mobilisation Device for the Knee
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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Software identification