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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

EK01.V02 — Class IIa MDR by Gondola Medical…

MD Atlas
Gondola Medical Technologies SA

EUDAMED last updated this device on May 12, 2026

EK01.V02

7649991214Gondola-EK018S

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Gondola Medical Technologies SA
UDI-DI code: 07649991214084
Reference / catalog number: EK01.V02

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Manufacturer information

Organization name: Gondola Medical Technologies SA
SRN: CH-MF-000015837
Manufacturer status: Active

Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	Jan 1, 2020	Still on market

Device identification

Trade name: not provided
UDI-DI code: 07649991214084
Basic UDI-DI: 7649991214Gondola-EK018S
Reference / catalog number: EK01.V02
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: Therapeutic device for the treatment of walking and balance impairments in patients with neurological disorders
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z129099VARIOUS INSTRUMENTS FOR FUNCTIONAL EXPLORATION AND THERAPEUTIC INTERVENTIONS - OTHER

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

EK01.V017649991214Gondola-EK018SOn 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.