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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

BeMate — Class I MDR by MULTIORTHOS LDA

MD Atlas
MULTIORTHOS LDA

EUDAMED last updated this device on May 11, 2026

BeMate

56001229140BMCPCFD

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MULTIORTHOS LDA
UDI-DI code: 05600371600851
Reference / catalog number: BMCPC40/40ABCA

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View device family (Basic UDI)

Manufacturer information

Organization name: MULTIORTHOS LDA
SRN: PT-MF-000044879
Manufacturer status: Active

Related devices

BeMate56001229140BMCPCFDOn the market BeMate56001229140BMCPCFDOn the market BeMate56001229140BMCPCFDOn the market BeMate56001229140BMCPCFDOn the market BeMate56001229140BMCPCFDOn 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

No critical warnings reported for this device.

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Market distribution

Primary placement in Portugal; available across 1 country total.

Country	On market since	Until
PortugalPrimary placement		Still on market

Device identification

Trade name: BeMate
UDI-DI code: 05600371600851
Basic UDI-DI: 56001229140BMCPCFD
Reference / catalog number: BMCPC40/40ABCA
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: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05600371600851

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Y180939MODULAR POSTURE SYSTEMS

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

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