florio PNH

Nom de l'organisation

Florio GmbH

SRN

DE-MF-000027001

Statut du fabricant

Actif

1 avertissement enregistré — faire défiler le panneau pour tout voir.

• CW011

  florio PNH is not intended to be used by patients with a disease other than PNH. Additionally, the patient must not be classified as a minor which is defined as those who have not reached the age of majority within their respective country. florio PNH is not intended to be used in place of advice from a Healthcare Professional (HCP). HCPs are required to exercise independent professional judgement at all times. HCPs are responsible for making decisions related to treatment regimenand would primarily rely on the patient’s individual medical records. Additionally, florio PNH is not an application to be used for reporting side effects of the medicines added and does not store or submit adverse event reports. Please consult your HCP with any questions or concerns you may have regarding your health condition. Relevant contact details of the manufacturer can be found on the manufacturers’ website which should be on any medicine packaging.

Marché principal en Allemagne ; disponible dans 16 pays au total.

Dénomination commerciale

florio PNH

Code d'UDI-DI

04260748180082

Basic UDI-DI

426074818florioPNH49

Numéro de référence/catalogue

not applicable

Entité d'attribution

GS1

Catégorie de risque

Classe I

Législation applicable

MDR [Règlement (UE) 2017/745 relatif aux dispositifs médicaux]

Statut

Sur le marché

Quantité

1

Description complémentaire du produit

iOS variant

URL des informations complémentaires

https://florio.com/florio-pnh-instructions-for-use/

Dimensions cliniques

Aucune dimension clinique enregistrée pour ce dispositif.

• V92MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES

• Numéro de lot
• Date d'expiration
• Date de fabrication
• Numéro de série
• Identification du logiciel