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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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ERMES_PLUS — 1 UDI-DI variant, MDR (Medico Srl)

MD Atlas
Medico Srl

Data from EUDAMED, last updated May 31, 2026

ERMES_PLUS

803292600RMMJ5

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Medico Srl

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 803292600RMMJ5
Device name: ERMES_PLUS
Device model: ERMES_PLUS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: Medico Srl
SRN: IT-MF-000016800
Country: Italy
Email: eudamed@medicoweb.com

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01KS2SG0QTPEVGR0DQFM6ZR9W2

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

ERMES_PLUS08032926007131