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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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Coni Auricolari — 16 UDI-DI variants, MDR (Eurosirel Spa)

MD Atlas
Eurosirel Spa

Data from EUDAMED, last updated May 30, 2026

Coni Auricolari

8017990COAFK

16 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: Eurosirel Spa

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8017990COAFK
Device name: Coni Auricolari
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 7, 2022

Manufacturer & authorised representative

Manufacturer

Name: Eurosirel Spa
SRN: IT-MF-000005982
Country: Italy
Email: m.lenti@eurosirel.it

Variants by status

UDI-DI variants

16 UDI-DI variants

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Applied filters

basicUdiUlid01G7BW6AB7G6S94WD1HQ3VHHZX

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

COA00954605948567009546
COA30044508000965300445
COA00435408056210004354
COA09245208057741092452
COA10066708008240100667
COA424350 08595566424350
COA41740608595566417406
COA33354008058951333540
COA00623608031377006236
COA00914808026486009148
LA NUOVA PHARMACIA08017596056962
COA00423708053046004237
COA16263408017990162634
COA62103908053298621039
COA08565008017990085650
COA72749208430321727492