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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

KinTracK version 2 — Class IIa MDR by EKINNOX

MD Atlas
EKINNOX

EUDAMED last updated this device on Feb 7, 2025

KinTracK version 2

3770017707019V

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: EKINNOX
UDI-DI code: 03770017707007
Reference / catalog number: KinTracK version 2

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Manufacturer information

Organization name: EKINNOX
SRN: FR-MF-000000917
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Jul 12, 2021	Aug 25, 2022

Device identification

Trade name: not provided
UDI-DI code: 03770017707007
Basic UDI-DI: 3770017707019V
Reference / catalog number: KinTracK version 2
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: KinTracK version 2
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12062582KINEMATIC MOTION CAPTURE ANALYSIS SYSTEMS - SOFTWARE ACCESSORIES

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

Related devices

KinTracK version 33770017707019VOn the market

Certificates

Certificate health across this manufacturer's portfolio.

G10 105291 0002Issued
Quality management systemNotified body: 0123Expiry: Jun 21, 2026