13001267

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 single-dose container to come into contact with the eye or other objects. • To avoid damage to the ocular surface, do not allow the single-dose container to come into contact with the eye while instilling the product. • The product is in single-dose packaging. After administration, the sealed single-dose container with the remaining content should be disposed of in accordance with local requirements. • The product is in single-dose packaging. The volume contained in the single-dose container is for a single administration, since the product does not contain preservatives. Reuse of the residual content may cause ophthalmic infection and/or patient injury. • No interactions of TRIUM MONODOSE 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 single-dose container or the aluminium pouch are damaged. • Keep the product out of 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.

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

Dénomination commerciale

non renseigné

Code d'UDI-DI

08055267241637

Basic UDI-DI

80336618004210200000000RH

Numéro de référence/catalogue

13001267

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

• 0.35 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.

• Q02030206EYE LUBRICANT SOLUTIONS