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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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Saljol Allround Rollator — 4 UDI-DI variants, MDR (Saljol GmbH)

MD Atlas
Saljol GmbH

Data from EUDAMED, last updated May 23, 2026

Saljol Allround Rollator

4058789SaljolAllroundEZ

4 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: Saljol GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4058789SaljolAllroundEZ
Device name: Saljol Allround Rollator
Device model: Saljol Allround Rollator
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 20, 2023

Manufacturer & authorised representative

Manufacturer

Name: Saljol GmbH
SRN: DE-MF-000015913
Country: Germany
Email: technik@saljol.de

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01H5Q9XE7HM4D12WM93058GFEY

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

Saljol Allround Rollator AR54 Pearl Grey04058789014059
Saljol Allround Rollator AR62 Magic Black04058789014042
Saljol Allround Rollator AR54 Magic Black04058789014066
Saljol Allround Rollator AR62 pearl grey04058789014271