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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

PL60/455007 — IVDR Class A IVDR by Plasticerveira -…

MD Atlas
Plasticerveira - Transformação de Plástico, Lda

EUDAMED last updated this device on Aug 8, 2024

PL60/455007

5600299202FA00042KF

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Plasticerveira - Transformação de Plástico, Lda
UDI-DI code: 05600299202335
Reference / catalog number: PL60/455007

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View device family (Basic UDI)

Manufacturer information

Organization name: Plasticerveira - Transformação de Plástico, Lda
SRN: PT-MF-000019369
Manufacturer status: Active

Related devices

PL09-04* 5600299202FA00041KDOn the market PL09-04-TA5600299202FA00041KDOn the market PL60I5005600299202FA00040KBOn the market PL03-0165-04 5600299202FA00038KQOn the market PL03-0164-04 5600299202FA00038KQOn the market

Critical warnings

No critical warnings reported for this device.

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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: 05600299202335
Basic UDI-DI: 5600299202FA00042KF
Reference / catalog number: PL60/455007
Issuing entity: GS1

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Kit para recolha, armazenamento e transporte de amostras de urina, 60ml
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

W05010203URINE COLLECTION, CONTAINERS

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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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.