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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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FEDMEDMICFIOT — 2 UDI-DI variants, MDR (Italeco S.r.l.)

MD Atlas
Italeco S.r.l.

Data from EUDAMED, last updated May 30, 2026

FEDMEDMICFIOT

805071388MICFIOTOYN

2 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: Italeco S.r.l.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805071388MICFIOTOYN
Device name: FEDMEDMICFIOT
Device model: Otoscope
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 3, 2023

Manufacturer & authorised representative

Manufacturer

Name: Italeco S.r.l.
SRN: IT-MF-000029458
Country: Italy
Email: info@italeco.com
Phone: +39 (0) 11 5690295

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GX32ZHZGTW20TGGYQ8MFY1E1

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

FEDMEDMICFIOT-U08050713880859
FEDMEDMICFIOT08050713880019