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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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e-motion M25 — 55 UDI-DI variants, MDR (Alber GmbH)

MD Atlas
Alber GmbH

Data from EUDAMED, last updated May 23, 2026

e-motion M25

4046727e-motionM258K

55 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: Alber GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 4046727e-motionM258K
Device name: e-motion M25
Device model: e-motion M25
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 31, 2025

Manufacturer & authorised representative

Manufacturer

Name: Alber GmbH
SRN: DE-MF-000005502
Country: Germany
Email: info@alber.de
Phone: +49 7432 2006 0

Variants by status

UDI-DI variants

55 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JJY7GAK551JQP2R56DAAFB4E

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

159267904046727186067
159269704046727186241
159266304046727185909
159265204046727185794
159269604046727186234

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