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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

1038780 — Class I MDR by FARMABAN s.a.

MD Atlas
FARMABAN s.a.

EUDAMED last updated this device on May 15, 2026

1038780

8428012CPKSPORT9D

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: FARMABAN s.a.
UDI-DI code: 08428012303452
Reference / catalog number: 1038780

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Manufacturer information

Organization name: FARMABAN s.a.
SRN: ES-MF-000004713
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.

Critical warnings

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

CW999
CONTRAINDICACIONES: No utilizar en caso de problemas arteriales, problemas vasculares graves y en caso de edema severo (a criterio del profesional médico). No utilizar en caso de hipersensibilidad conocida a alguno de sus componentes. PRECAUCIONES: No aplicar sobre heridas abiertas y/o zonas de punción. No introducir el producto sin esterilizar en zonas estériles. No aplicar con demasiada tensión. En caso de desarrollar dolor, palidez, enfriamiento o adormecimiento retirar el vendaje inmediatamente. Si el dolor persiste o en caso de situaciones adversas consultar con el farmacéutico, fisioterapeuta o profesional médico.

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08428012303452
Basic UDI-DI: 8428012CPKSPORT9D
Reference / catalog number: 1038780
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: Venda cohesiva elástica Everest
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 7.5 MU10
4.5 MU36
Verde

EMDN nomenclature code(s)

M030499ELASTIC BANDAGES, SUPPORT AND COMPRESSION - OTHER
M03030199ELASTIC FIXING BANDAGES - 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