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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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Saalux UV Kamm (UVB 311nm) DE — 2 UDI-DI variants, MDR

MD Atlas
Saalmann medical GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Saalux UV Kamm (UVB 311nm) DE

426058751SAALUXDK

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Saalmann medical GmbH & Co. KG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426058751SAALUXDK
Device name: Saalux UV Kamm (UVB 311nm) DE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 13, 2025

Manufacturer & authorised representative

Manufacturer

Name: Saalmann medical GmbH & Co. KG
SRN: DE-MF-000010552
Country: Germany
Email: info@saalmann-medical.de
Phone: +49 5731 254500

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01K9YRYT4DF0JF2W2GY2PH1VSK

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

07-02-000-0304260587511030
07-02-000-0104260587511016