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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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Electric medical bed — 3 UDI-DI variants, MDR (Burmeier GmbH & Co. KG)

MD Atlas
Burmeier GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Electric medical bed

4047037Regia8W

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: Burmeier GmbH & Co. KG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 4047037Regia8W
Device name: Electric medical bed
Device model: Regia
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 16, 2025

Manufacturer & authorised representative

Manufacturer

Name: Burmeier GmbH & Co. KG
SRN: DE-MF-000010563
Country: Germany
Email: info@burmeier.de
Phone: +49 (0) 5232 9841 - 0

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JVBQNATZTT2SS4GB9739WSZ3

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

30006904047037900329
30006904047037900046
30006904047037900312