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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

RUWP500 — Class I MDR by Reintex GmbH

MD Atlas
Reintex GmbH

EUDAMED last updated this device on Apr 29, 2026

RUWP500

426243112RTBETTSET16P

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Reintex GmbH
UDI-DI code: 04262431120771
Reference / catalog number: RUWP500

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Manufacturer information

Organization name: Reintex GmbH
SRN: DE-MF-000041775
Manufacturer status: Active

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2042B426243112RTBETTSET16POn the market 2042W426243112RTBETTSET16POn the market RTUBT/S 426243112RTUMBETT2GOn the market RTBK40426243112RTBETTSET16POn the market RTBK60426243112RTBETTSET16POn the market

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.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jul 1, 2024	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04262431120771
Basic UDI-DI: 426243112RTBETTSET16P
Reference / catalog number: RUWP500
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: —
Additional information URL: https://www.reintex.com/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V08068099MEDICAL BEDS - OTHER ACCESSORIES

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
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Software identification