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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

M3D BM Light SLS — Class I MDR by Rehadapt GmbH

MD Atlas
Rehadapt GmbH

EUDAMED last updated this device on Mar 18, 2024

M3D BM Light SLS

++B896BEDMOUNTSGR

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Rehadapt GmbH
UDI-DI code: +B89620132502
Reference / catalog number: 20.1325

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Manufacturer information

Organization name: Rehadapt GmbH
SRN: DE-MF-000008141
Manufacturer status: Active

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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.

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: M3D BM Light SLS
UDI-DI code: +B89620132502
Basic UDI-DI: ++B896BEDMOUNTSGR
Reference / catalog number: 20.1325
Issuing entity: HIBCC

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: M3D bedmount for light devices such as switches or environmental controls. Tube lengths 200 x 300 mm (8 x 12"). QuickShift joints and receiver for the SLS connection. Max. load capacity: 1.2 kg (2.6 lbs). Compatible with Rehadapt Care Bed frame clamps (not included).
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y214299DEVICES FOR INTERPERSONAL COMUNICATION - OTHER

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

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Manufacturing date
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Software identification