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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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Cono per l’igiene dell’orecchio — 3 UDI-DI variants, MDR (Aurora Srl)

MD Atlas
Aurora Srl

Data from EUDAMED, last updated May 30, 2026

Cono per l’igiene dell’orecchio

8017690CONESX6

3 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Aurora Srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8017690CONESX6
Device name: Cono per l’igiene dell’orecchio
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 24, 2025

Manufacturer & authorised representative

Manufacturer

Name: Aurora Srl
SRN: IT-MF-000018589
Country: Italy
Email: d.settanni@aurorasrl.net
Phone: +39 0543 724987

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FZ8747A3TWESWTPWJSYYHN48

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

211040308408017690000090
202010007508017690000045
239010312008029241103068