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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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Paingone Plus — 3 UDI-DI variants, MDR (ITALRES SRL)

MD Atlas
ITALRES SRL

Data from EUDAMED, last updated May 30, 2026

Paingone Plus

80538482120DM6E

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: ITALRES SRL

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 80538482120DM6E
Device name: Paingone Plus
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: ITALRES SRL
SRN: IT-MF-000029584
Country: Italy
Email: info@italres.com
Phone: +39-055-452322

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KQRZ28XH6HMJ03BMJSGAGC9M

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

Paingone Plus08053848210010
Paingone Plus08053848210058
20DM08053848210065