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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

Finbo XL — Class I MDR by M.Ex.T. Belgium

MD Atlas
M.Ex.T. Belgium

EUDAMED last updated this device on Mar 30, 2026

Finbo XL

54009380003-BAJ9

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: M.Ex.T. Belgium
UDI-DI code: 05400938000205
Reference / catalog number: 0010.901

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Manufacturer information

Organization name: M.Ex.T. Belgium
SRN: BE-MF-000022927
Manufacturer status: Active

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Critical warnings

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

CW007
Do not use if package is damaged

Market distribution

Primary placement in Belgium; available across 3 countries total.

Country	On market since	Until
BelgiumPrimary placement		Still on market
Germany		Still on market
Netherlands		Still on market

Device identification

Trade name: Finbo XL
UDI-DI code: 05400938000205
Basic UDI-DI: 54009380003-BAJ9
Reference / catalog number: 0010.901
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: 5
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)

M03030103TUBULAR NET BANDAGES

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.