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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

MoVeS Bar | Extra Light - Tan — Class I MDR by MVS In Motion

MD Atlas
MVS In Motion

EUDAMED last updated this device on May 20, 2026

MoVeS Bar | Extra Light - Tan

542006300A2X

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MVS In Motion
UDI-DI code: 05420063003476
Reference / catalog number: 01-600101

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Manufacturer information

Organization name: MVS In Motion
SRN: BE-MF-000000664
Manufacturer status: Active

Related devices

03-050101542006300G3BOn the market 01-200305542006300A2XOn the market 01-200304542006300A2XOn the market 01-200302542006300A2XOn the market 01-200303542006300A2XOn the market

Critical warnings

3 warnings recorded — scroll inside the panel to see all entries.

CW030
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW083
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Belgium; available across 1 country total.

Country	On market since	Until
BelgiumPrimary placement		Still on market

Device identification

Trade name: MoVeS Bar | Extra Light - Tan
UDI-DI code: 05420063003476
Basic UDI-DI: 542006300A2X
Reference / catalog number: 01-600101
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.

EMDN nomenclature code(s)

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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.