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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

494302-801113 — Class I MDR by Tecnoclínic SA

MD Atlas
Tecnoclínic SA

EUDAMED last updated this device on Aug 2, 2024

494302-801113

843657368BCONSTNG

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Tecnoclínic SA
UDI-DI code: 08470004943023
Reference / catalog number: 494302-801113

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Manufacturer information

Organization name: Tecnoclínic SA
SRN: ES-MF-000000632
Manufacturer status: Active

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
* No utilizar como instrumento de medición. * La reutilización de la bolsa podría comportar riesgo de infección. * Se debe sustituir la bolsa antes de alcanzar el nivel máximo. * La bolsa colectora debe ser siempre colgada de un soporte, situándola por debajo del nivel de la vejiga urinaria para evitar reflujo. * Fijar firmemente el conector a la sonda o adaptador penil. * Evitar aplastar, pinzar o colapsar el tubo durante la utilización del producto para no interrumpir el flujo de la orina hacia la bolsa. * Vaciar la bolsa en el WC antes de descartarla en un contenedor de residuos, de acuerdo con las disposiciones vigentes.

Market distribution

Primary placement in Spain; available across 1 country total.

Placed on the market in Spain; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 08470004943023
Basic UDI-DI: 843657368BCONSTNG
Reference / catalog number: 494302-801113
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: 30
Additional product description: Bolsa colectora de orina de cama
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A06030301URINE COLLECTION BAGS

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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