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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 Standard, rot — 3 UDI-DI variants, MDR (Ludwig Bertram GmbH)

MD Atlas
Ludwig Bertram GmbH

Data from EUDAMED, last updated May 23, 2026

Rollator Standard, rot

4048792MO01001FR

3 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: Ludwig Bertram GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4048792MO01001FR
Device name: Rollator Standard, rot
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: Ludwig Bertram GmbH
SRN: DE-MF-000013037
Country: Germany
Email: info@bertram.de
Phone: +49513697590

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KRNC7BWYPCA60WF8HD0959JK

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

1144202004048792004819
1144203504048792004833
1144243504048792039385