13001252

Nom de l'organisation

Fidia Farmaceutici S.p.A.

SRN

IT-MF-000026988

Statut du fabricant

Actif

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

• CW999

  • The product is for ophthalmic external use only (eye surface). • In order to avoid the risk of cross-infection, the product is intended to be used by a single patient only. • To avoid contaminating the solution, do not allow the dropper to come into contact with the eye or other objects. • To avoid damage to the ocular surface, do not allow the dropper to come into contact with the eye while instilling the product. • As the solution in the bottle runs out, greater pressure will need to be applied for the drop to be dispensed. It is recommended that the optimum pressure is determined to avoid dispensing more than the amount indicated. • Close the bottle tightly after use. The cap has an inside coating that absorbs any residual drop. • No interactions of FIDIALEYE NORM with drugs or other topical ophthalmic products are known; however, consult your physician in case of concomitant administration with other topical ophthalmic products for specific indications on timing of administration. • Do not use the product if the bottle is damaged. • Keep the product out of the sight and reach of children. • In case of any undesirable effects, discontinue use and seek medical advice. • Keep the box and the leaflet for the entire period of use of the device. • Dispose of the sealed bottle with the remaining content according to your local waste management regulations.

Marché principal en Espagne ; disponible dans 1 pays au total.

Dénomination commerciale

non renseigné

Code d'UDI-DI

08055267241460

Basic UDI-DI

80336618004060100000000TB

Numéro de référence/catalogue

13001252

Entité d'attribution

GS1

Catégorie de risque

Classe IIb

Législation applicable

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

Statut

Sur le marché

Quantité

1

Description complémentaire du produit

—

URL des informations complémentaires

Aucune URL d'informations complémentaires renseignée par le fabricant.

Dimensions cliniques

• 2 MU48

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

Nomenclature européenne des dispositifs médicaux — la classification produit UE attribuée à ce dispositif.

• Q0299OPHTHALMIC DEVICES - OTHER