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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

Z1020S — Class I MDR by ALGRAN MANUFACTURA…

MD Atlas
ALGRAN MANUFACTURA SANITARIA, S.L.

EUDAMED last updated this device on May 3, 2026

Z1020S

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: 08437013599207
Reference / catalog number: Z1020S

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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, 2046

Device identification

Trade name: not provided
UDI-DI code: 08437013599207
Basic UDI-DI: 8437013CBTLOUR
Reference / catalog number: Z1020S
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

Related devices

Z1020XL8437013CBTLOUROn the market Z1020L8437013CBTLOUROn the market Z1020M8437013CBTLOUROn the market Z1020XS8437013CBTLOUROn the market Z10010L8437013CBTRJUZOn 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.