447902

Organization name

BD Kiestra B.V.

SRN

NL-MF-000018863

Manufacturer status

Active

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

• CW007

  EUDAMED did not publish a description for this code.
• CW011

  EUDAMED did not publish a description for this code.
• CW010

  EUDAMED did not publish a description for this code.
• CW999

  Ayrı olarak toplayın Elektrikli ve elektronik ekipman atıklarının ayrı olarak toplanmasının gerekli olduğunu belirtir.
• CW999

  Indsamles separat Angiver, at særskilt indsamling af affald fra elektrisk og elektronisk udstyr er påkrævet.
• CW999

  Getrennt sammeln Zeigt an, dass eine getrennte Sammlung für Abfälle aus Elektro- und Elektronikgeräten erforderlich ist.
• CW999

  Recoger por separado Indica la recogida separada de residuos de equipos eléctricos y electrónicos requerida.
• CW999

  Collecter séparément Indique qu'une collecte séparée des déchets d'équipements électriques et électroniques est requise.
• CW999

  Recolher separadamente Indica a necessidade de recolha separada de resíduos de equipamentos elétricos e eletrónicos.
• CW999

  Raccogliere separatamente Indica la raccolta separata dei rifiuti di apparecchiature elettriche ed elettroniche richiesta.
• CW999

  Apart inzamelen Geeft aan dat aparte inzameling vereist is voor afval van elektrische en elektronische apparatuur.
• CW999

  Samle separat Indikerer at separat innsamling for elektrisk og elektronisk avfall er påkrevd.
• CW999

  Kerää erikseen Ilmaisee, että sähkö- ja elektroniikkalaitteiden jätteiden erilliskeräys on pakollista.
• CW999

  Samla separat Indikerar att separat insamling av avfall från elektrisk och elektronisk utrustning krävs.
• CW999

  Collect separately Indicates separate collection for waste of electrical and electronic equipment required.

Primary placement in Belgium; available across 1 country total.

Trade name

not provided

UDI-DI code

00382904479022

Basic UDI-DI

038290IAVSLVOZEG

Reference / catalog number

447902

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

1

Additional product description

—

Additional information URL

https://www.bd.com/e-labeling

Clinical sizes

No clinical sizes registered for this device.

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

• W02039080VARIOUS MICROBIOLOGY INSTRUMENTS - HARDWARE ACCESSORIES