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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

ARTEMIS — Class IIa MDD by NOVAVISION GROUP

MD Atlas
NOVAVISION GROUP

EUDAMED last updated this device on Dec 1, 2025

ARTEMIS

B-08059340930302

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: NOVAVISION GROUP
UDI-DI code: 08059340930302
Reference / catalog number: 380800000333

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View device family (Basic UDI)

Manufacturer information

Organization name: NOVAVISION GROUP
SRN: IT-MF-000024333
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	Dec 1, 2021	Still on market

Device identification

Trade name: ARTEMIS
UDI-DI code: 08059340930302
Basic UDI-DI: B-08059340930302
Reference / catalog number: 380800000333
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: ARTEMIS is a radiofrequency generator suitable for non-invasive application in procedures for the treatment of: o adiposis edematosa (pathology caused by alteration of the subcutaneous or hypodermic tissue with hypertrophy of the adipose cells)
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08059340930302

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Z12040203DERMAL REGENERATION 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

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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.