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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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Reha-Schwerlastbett 280/400 — 2 UDI-DI variants, MDR

MD Atlas
RFH - Rehatechnik GmbH

Data from EUDAMED, last updated May 23, 2026

Reha-Schwerlastbett 280/400

42518952014PH

2 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: RFH - Rehatechnik GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 42518952014PH
Device name: Reha-Schwerlastbett 280/400
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 30, 2025

Manufacturer & authorised representative

Manufacturer

Name: RFH - Rehatechnik GmbH
SRN: DE-MF-000007015
Country: Germany
Email: kontakt@rfh-rehatechnik.de
Phone: +49 (0) 921 151 100 60

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K62T9NGPY4K97ST0A84EKP7J

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

Rehab heavy duty bed 280/40004251895200143
Rehab upholstered bed04251895200150