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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

C3 — Class I MDR by MOBI-ENDOS,S.L.

MD Atlas
MOBI-ENDOS,S.L.

EUDAMED last updated this device on Jan 18, 2026

C3

84370243371cartptx5G

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MOBI-ENDOS,S.L.
UDI-DI code: 08437024337188
Reference / catalog number: C3

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Manufacturer information

Organization name: MOBI-ENDOS,S.L.
SRN: ES-MF-000021771
Manufacturer status: Active

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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 Spain; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 08437024337188
Basic UDI-DI: 84370243371cartptx5G
Reference / catalog number: C3
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: C3 _ Carro accesorio para ubicar y desplazar equipos de endoscopia y laparoscopia RICHARD WOLF y otros, Accesorios opcionales disponibles: Brazo monitor MH4.1: REFª MH4.1 Brazo monitor MH4,1/7: REFª MH4.1/7 Soporte botella SB24154: REFª SB24154 Soporte monitor rígido MB385: REFª MB385.1 Conjunto soporte colgador 2 video-endoscopia: REFª CE+TS
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z129099VARIOUS INSTRUMENTS FOR FUNCTIONAL EXPLORATION AND THERAPEUTIC INTERVENTIONS - 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

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Expiration date
Manufacturing date
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Software identification