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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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Aquolab OzoActive — 3 UDI-DI variants, MDR (EB2C Srl)

MD Atlas
EB2C Srl

Data from EUDAMED, last updated May 30, 2026

Aquolab OzoActive

805534992-AQ-OZOACTIVEXP

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: EB2C Srl

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805534992-AQ-OZOACTIVEXP
Device name: Aquolab OzoActive
Device model: AQ.OA-0045
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 14, 2023

Manufacturer & authorised representative

Manufacturer

Name: EB2C Srl
SRN: IT-MF-000019583
Country: Italy
Email: germini@eb2c.it
Phone: +39 02 3668 6416

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H7SY26W6BYHMTJ4CMDBCTH2B

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

AQ.OA-004508055349923413
AQ.OA-PR004008055349923390
AQ.OA-OS003908055349923376