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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

Z1020M — Class I MDR by ALGRAN MANUFACTURA…

MD Atlas
ALGRAN MANUFACTURA SANITARIA, S.L.

EUDAMED last updated this device on May 3, 2026

Z1020M

8437013CBTLOUR

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ALGRAN MANUFACTURA SANITARIA, S.L.
UDI-DI code: 08437013599191
Reference / catalog number: Z1020M

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Manufacturer information

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

Related devices

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Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement	May 11, 2013	Dec 30, 2046

Device identification

Trade name: not provided
UDI-DI code: 08437013599191
Basic UDI-DI: 8437013CBTLOUR
Reference / catalog number: Z1020M
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: Inmovilización y estabilización de mano, brazo y hombro. INSTRUCCIONES DE USO: Usuario previsto de este producto será por un profesional sanitario. • Deslice el extremo abierto de la cinta sobre la mano del lado lesionado • Ajustar el cabestrillo en su brazo de manera que el codo quede en la parte mas trasera del inmovilizador y coloque el pulgar en la presilla. • Coloque la cinta de sujeción alrededor de su cuello y ajuste mediante el cierre de velcro a la longitud deseada. • Ajuste el cinturón al tamaño deseado.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y060699ORTHOSES, UPPER EXTREMITY - 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

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.