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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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Reverse osmosis deionizer — 3 UDI-DI variants, IVDR

MD Atlas
Quality Invents srl

Data from EUDAMED, last updated May 30, 2026

Reverse osmosis deionizer

8057971318057971310005S2

3 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Quality Invents srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8057971318057971310005S2
Device name: Reverse osmosis deionizer
Device model: DIA CLASS
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Sep 20, 2022

Manufacturer & authorised representative

Manufacturer

Name: Quality Invents srl
SRN: IT-MF-000028649
Country: Italy
Email: amministrazione@quality-group.eu

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01GDDQ3925PQF7SK1CJX9B4G4D

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

Q-1020-0508057971310050
Q-1020-0708057971310036
Q-1020-0608057971310043