127

Organization name

BIODISIN S.R.L

SRN

IT-MF-000031661

Manufacturer status

Active

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

• CW265

  EUDAMED did not publish a description for this code.
• CW041

  EUDAMED did not publish a description for this code.
• CW073

  EUDAMED did not publish a description for this code.
• CW081

  EUDAMED did not publish a description for this code.
• CW167

  EUDAMED did not publish a description for this code.
• CW193

  EUDAMED did not publish a description for this code.
• CW194

  EUDAMED did not publish a description for this code.
• CW430

  EUDAMED did not publish a description for this code.
• CW444

  EUDAMED did not publish a description for this code.
• CW397

  EUDAMED did not publish a description for this code.
• CW416

  EUDAMED did not publish a description for this code.
• CW225

  EUDAMED did not publish a description for this code.
• CW035

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

  Uso esclusivamente professionale. Non miscelare con altre sostanze. Evitare il contatto con occhi e pelle. Usare DPI idonei. Utilizzare in lavastrumenti con sistema di pescaggio automatico. Il prodotto ALCAWASH è stato sviluppato per un uso esclusivamente professionale. Prodotto monouso. Nell’utili- zzo seguire le avvertenze riportate in etichetta e nella scheda di sicurezza. L’utilizzatore e/o il paziente deve segnalare qualsiasi incidente grave verificatori in relazione al dispositivo al fabbricante e all’autorità competente dello stato membro in cui l’utilizzatore e/o il paziente è stabilito.

Primary placement in Italy; available across 1 country total.

Trade name

not provided

UDI-DI code

08055712800556

Basic UDI-DI

805571280AlcawashAV

Reference / catalog number

127

Issuing entity

GS1

Risk category

Class I

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

Alcawash 5L

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

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

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

• D0899DETERGENTS FOR MEDICAL DEVICES - OTHER