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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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EPS-P10 — 1 UDI-DI variant, MDR

MD Atlas
MRC Systems GmbH Medizintechnische Systeme

Data from EUDAMED, last updated May 31, 2026

EPS-P10

426235523EPS-P108W

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: MRC Systems GmbH Medizintechnische Systeme

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426235523EPS-P108W
Device name: —
Device model: EPS-P10
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 4, 2025

Manufacturer & authorised representative

Manufacturer

Name: MRC Systems GmbH Medizintechnische Systeme
SRN: DE-MF-000011848
Country: Germany
Email: info@mrc-systems.de
Phone: +49 6221 1380300

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01K96XEV0DZ0KYHHJ1NTJP5NKC

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

EPS-P1004262355231003