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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

TRI BIKE E-CLASSIC S MID — Class I MDR by MOBILE-TECHNICS BV

MD Atlas
MOBILE-TECHNICS BV

EUDAMED last updated this device on Mar 5, 2026

TRI BIKE E-CLASSIC S MID

540701126E-CLASSICSMID09K

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MOBILE-TECHNICS BV
UDI-DI code: 05407011260235
Reference / catalog number: TRI BIKE E-CLASSIC S MID

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Manufacturer information

Organization name: MOBILE-TECHNICS BV
SRN: BE-MF-000037911
Manufacturer status: Active

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TRI BIKE FROGGY SMALL540701126FROGGYSMALL00056On the market TRI BIKE ECO TRIKE S24540701126ECOTRIKES24000C9On the market TRI BIKE E-CLASSIC S540701126E-CLASSICS0000VTOn the market TRI BIKE FROGGY540701126FROGGY00000000C8On the market TRI BIKE CLASSIC Y COMFORT 540701126CLASSICYCOMF00NDOn 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.

Market distribution

Primary placement in Belgium; available across 1 country total.

Placed on the market in Belgium; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 05407011260235
Basic UDI-DI: 540701126E-CLASSICSMID09K
Reference / catalog number: TRI BIKE E-CLASSIC S MID
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: DRIEWIELFIETS VOOR VOLWASSENEN
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y99DEVICES FOR PERSONS WITH DISABILITIES NOT INCLUDED IN OTHER CATEGORIES - 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
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Software identification