Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

Z2626XXL — Class I MDR by ALGRAN MANUFACTURA…

MD Atlas
ALGRAN MANUFACTURA SANITARIA, S.L.

EUDAMED last updated this device on May 15, 2026

Z2626XXL

8437013SPTUN67

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ALGRAN MANUFACTURA SANITARIA, S.L.
UDI-DI code: 08437013599337
Reference / catalog number: Z2626XXL

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

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

Related devices

Z1020XL8437013CBTLOUROn the market Z1020L8437013CBTLOUROn the market Z1020M8437013CBTLOUROn the market Z1020S8437013CBTLOUROn the market Z1020XS8437013CBTLOUROn 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.

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: 08437013599337
Basic UDI-DI: 8437013SPTUN67
Reference / catalog number: Z2626XXL
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 del tórax en pacientes sometidos a esternotomías. INSTRUCCIONES DE USO: • Coloque el soporte esternal extendido sobre la cama, con la etiqueta del fabricante mirando hacia abajo y los tirantes desabrochados y extendidos. • Coloque al paciente sobre el soporte, asegurándose de que esta bien centrado. • Si el paciente esta encamado, levante ligeramente su cabeza y tronco y deslice el soporte debajo. • Cierre los velcros del soporte ajustándolo al tamaño adecuado asegurase de que las barras laterales quedan a ambos lados de la herida esternal. • Pase los tirantes sobre los hombros del paciente y fíjelos sobre la parte central del soporte a la altura dehesada • Durante el acceso de tos, estornudos u otros movimientos bruscos, sujete las asas integradas con una o dos manos y acérquelas entre si. Esto aumentara la tensión sobre el tórax proporcionando un soporte adicional.
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