AFB SAFEBAG KV

Organization name

Vantive Health GmbH

SRN

CH-MF-000038981

Manufacturer status

Active

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

• CW009

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

  EUDAMED did not publish a description for this code.
• CW020

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

  EUDAMED did not publish a description for this code.
• CW007

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

  DO NOT use unless the solution is clear and free from visible particles.
• CW999

  NO lo use a menos que la solución esté transparente y sin partículas visibles.
• CW999

  NE PAS utiliser à moins que la solution ne soit limpide et exempte de particules visibles.
• CW999

  NON utilizzare a meno che la soluzione non sia limpida e priva di particelle visibili.
• CW999

  To be used under medical supervision
• CW999

  Debe utilizarse bajo control médico.
• CW999

  A utiliser sous surveillance médicale.
• CW999

  Da utilizzare sotto la supervisione di un medico.
• CW999

  Not for Infusion.
• CW999

  No debe utilizarse para infusión.
• CW999

  Ne pas utiliser en perfusion.
• CW999

  Non destinato all’infusione.
• CW999

  Make sure that the composition corresponds to physician’s prescription
• CW999

  Asegúrese de que la composición corresponde a la prescripción del médico
• CW999

  Assurez-vous que la composition correspond à la prescription du médecin
• CW999

  Assicurarsi che la composizione corrisponda alla prescrizione del medico

Primary placement in Italy; available across 3 countries total.

Trade name

AFB SAFEBAG KV

UDI-DI code

07332414066017

Basic UDI-DI

7332414VA0000412V

Reference / catalog number

106890

Issuing entity

GS1

Risk category

Class IIb

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

—

Additional information URL

https://www.vantive.com/

Clinical sizes

• 5500 MU48

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

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

• F040302DIALYSIS CONCENTRATES, WITHOUT ACETATE BUFFER - AFB