CUP F/VACUUM COLLEC.120 ML PP I/B

Organization name

Deltalab, S.L.

SRN

ES-MF-000000153

Manufacturer status

Active

Certificate health across this manufacturer's portfolio.

2 warnings recorded — scroll inside the panel to see all entries.

• CW010

  • Be careful when handling the lid of the container which is containing a needle under the label. Risk of puncture. • Not suitable for any application other than its intended use. • Do not squeeze or press the container. • Do not use if package is damaged. • Do not use if, when removing the label from the lid, the needle that forms the transfer system for sample extraction is broken or bent. • Do not re-use. The re-use of this product may affect the subsequent analysis of the sample taken. • Do not use if printed product information is not displayed correctly. • Do not use if the expiry date is exceeded. • Discard the product if it is dirty.
• CW011

  Healthcare professionals must validate the use of the container for their specific assay instrument/reagent system combinations and specimen storage conditions.

Primary placement in Spain; available across 17 countries total.

Trade name

CUP F/VACUUM COLLEC.120 ML PP I/B

UDI-DI code

08435263848601

Basic UDI-DI

84356058UDI-DI-2166

Reference / catalog number

408726

Issuing entity

GS1

Risk category

IVDR Class A

Applicable legislation

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]

Status

On the market

Quantity

350

Additional product description

—

Additional information URL

https://www.deltalabgroup.com/eifus

Clinical sizes

No clinical sizes registered for this device.

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

• W05010203URINE COLLECTION, CONTAINERS