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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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ARTEMIS — 1 UDI-DI variant, MDD (NOVAVISION GROUP )

MD Atlas
NOVAVISION GROUP

Data from EUDAMED, last updated May 31, 2026

ARTEMIS

B-08059340930302

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIa

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: NOVAVISION GROUP

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Device characteristics

Active device

Legacy certificates

Certificate number: MED 31145
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: KIWA CERMET ITALIA S.P.A. (0476)
Validity: Oct 9, 2023

Identity & classification

Basic UDI-DI: B-08059340930302
Device name: ARTEMIS
Device model: Radiofrequancy Medical Device
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: Dec 1, 2025

Manufacturer & authorised representative

Manufacturer

Name: NOVAVISION GROUP
SRN: IT-MF-000024333
Country: Italy
Email: info@novavision.net
Phone: +39 0296720240

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KBCN6SWPX0AK1YPRVZYBKZ53

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

ARTEMIS08059340930302