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Organization name
UDI-DI code
Reference / catalog number

Z2525M — Class I MDR by ALGRAN MANUFACTURA…

MD Atlas
ALGRAN MANUFACTURA SANITARIA, S.L.

EUDAMED last updated this device on May 15, 2026

Z2525M

8437013SPTES4Z

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ALGRAN MANUFACTURA SANITARIA, S.L.
UDI-DI code: 08437013599313
Reference / catalog number: Z2525M

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Manufacturer information

Organization name: ALGRAN MANUFACTURA SANITARIA, S.L.
SRN: ES-MF-000042506
Manufacturer status: Active

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement	May 11, 2013	Dec 30, 2050

Device identification

Trade name: not provided
UDI-DI code: 08437013599313
Basic UDI-DI: 8437013SPTES4Z
Reference / catalog number: Z2525M
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: FINALIDAD: Inmovilización y estabilización de tórax y mamas en pacientes sometidos a esternotomías. INSTRUCCIONES DE USO: • Si la paciente esta encamada, levante ligeramente su cabeza y deslice bajo su tórax el soporte esternal con los tirantes desabrochados. • Ajuste los velcros laterales tamaño adecuado, asegurándose de que la cremallera de apertura queda centrada sobre la herida esternal. • Pase los tirantes sobre los hombros del pacientes y fijemos sobre la parte central del soporte a la altura deseada. • Si la paciente tiene cierta movilidad deslice sus brazos a través de las aberturas del soporte como haría con un sostén corriente y ajuste los velcros laterales y superiores según la tensión requerida. • Para acceder a la herida esternal, abra la cremallera central del soporte.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y060307THORACIC ORTHOSES

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

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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.