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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

7000-xx-xx / Pro — Class I MDR by FMB Care GmbH

MD Atlas
FMB Care GmbH

EUDAMED last updated this device on Apr 30, 2026

7000-xx-xx / Pro

PP10364CAREBED03

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: FMB Care GmbH
UDI-DI code: 111683105196
Reference / catalog number: 7000-xx-xx / Pro

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Manufacturer information

Organization name: FMB Care GmbH
SRN: DE-MF-000005985
Manufacturer status: Active

Related devices

7000-xx-xx /_EcoPP10364CAREBED03On the market 7000-xx-xx /_FirstPP10364CAREBED03On the market 7000-xx-xx / Pro+PP10364CAREBED03On the market 7000-xx-xx /_UltraLowPP10364CAREBED03On 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.

Critical warnings

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

CW010
Gebrauchsanweisung beachten / Voraussetzung um Gefahren zu vermeiden ist die richtige Montage und Bedienung des Bettes lt. Gebrauchsanweisung

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 111683105196
Basic UDI-DI: PP10364CAREBED03
Reference / catalog number: 7000-xx-xx / Pro
Issuing entity: IFA

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://fmb-care.de/ueber-uns/downloads/
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