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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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ARTE MOTORE DA 120 — 1 UDI-DI variant, MDR (NOI DELLA NOTTE SRL)

MD Atlas
NOI DELLA NOTTE SRL

Data from EUDAMED, last updated May 31, 2026

ARTE MOTORE DA 120

80575070250014PF

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: NOI DELLA NOTTE SRL

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 80575070250014PF
Device name: ARTE MOTORE DA 120
Device model: ARTE MOTORE DA 120
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: NOI DELLA NOTTE SRL
SRN: IT-MF-000048624
Country: Italy
Email: paolo.pasquini@noidellanotte.it
Phone: +390577684269

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01KS82MP24FYK3B7G2DQBES06S

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

ARTE MOTORE DA 12080575070250144