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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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Organization name
UDI-DI code
Reference / catalog number

Rehab bed 30.500 — Class I MDR by RFH - Rehatechnik GmbH

MD Atlas
RFH - Rehatechnik GmbH

EUDAMED last updated this device on Oct 6, 2025

Rehab bed 30.500

42518952017PP

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: RFH - Rehatechnik GmbH
UDI-DI code: 04251895200174
Reference / catalog number: Rehab bed 30.500

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Manufacturer information

Organization name: RFH - Rehatechnik GmbH
SRN: DE-MF-000007015
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: Rehab bed 30.500
UDI-DI code: 04251895200174
Basic UDI-DI: 42518952017PP
Reference / catalog number: Rehab bed 30.500
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: The RFH Pflegebett 30.500 is an electric care bed designed for homecare and clinical settings, combining comfort, safety and versatile adjustability.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V08060101HOSPITAL/HOME CARE ELECTRIC MEDICAL BEDS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.