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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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Rollator Aluminum range — 6 UDI-DI variants, MDR (by ACRE Aps)

MD Atlas
by ACRE Aps

Data from EUDAMED, last updated May 23, 2026

Rollator Aluminum range

57135041B3

6 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: by ACRE Aps

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 57135041B3
Device name: Rollator Aluminum range
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: by ACRE Aps
SRN: DK-MF-000010025
Country: Denmark
Email: contact@byacre.com
Phone: +4533445544

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KCPCVB30G54NJ1979FZPXPGZ

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

NP - M Army05713504005789
NP - M Baltic Blue05713504005802
NP - M Color Rush05713504005772
NP - M Glacier Green05713504005758
NP - M Granite Black05713504005765
NP - M Navy05713504005796