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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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GENERATORE DI OZONO SERIE E — 3 UDI-DI variants, MDR (Eco3 S.r.l.)

MD Atlas
Eco3 S.r.l.

Data from EUDAMED, last updated May 31, 2026

GENERATORE DI OZONO SERIE E

805620936SERIE_EUE

3 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Eco3 S.r.l.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805620936SERIE_EUE
Device name: GENERATORE DI OZONO SERIE E
Device model: E100, E80, E30
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 9, 2026

Manufacturer & authorised representative

Manufacturer

Name: Eco3 S.r.l.
SRN: IT-MF-000027945
Country: Italy
Email: eco3ozono@ozonline.it
Phone: +39 11 913 96 73

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KEH7H8PH7MJADFAEHJCDPTZ0

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

0100308056209360010
0300308056209360034
0800308056209360089