LUBRI EYES

Nom de l'organisation

C.O.C. FARMACEUTICI S.R.L.

SRN

IT-MF-000019321

Statut du fabricant

Actif

17 avertissements enregistrés — faire défiler le panneau pour tout voir.

• CW999

  It is necessary to report any serious incident occurred in relation to the device to the manufacturer and the Competent authority of the Member state in which you are established.
• CW999

  If you suffer from severe damage to the clear layer at the front of the eye (the cornea), phosphates may cause in very rare cases cloudy patches on the cornea due to calcium build-up during treatment
• CW262

  Strictly personal use only [EN]
• CW999

  During application, do not touch the eye or any other surface with the tip of the applicator
• CW999

  Ophthalmic use only
• CW007

  Do not use the product if the container is damaged or unsealed when first purchased [EN]
• CW999

  Do not use if are visible particles and/or changes in the color of the solution
• CW999

  Do not use in case of known incompatibility towards any of the components of the solution and/or Asteraceae plants and/or Malvacee plants
• CW999

  The product is not suitable for children
• CW036

  No interactions with drugs or other eye drops are reported; however, leave at least 15 minutes between administrations of any other eye drops [EN]
• CW277

  If side effects occur during use, stop using the product and consult a doctor [EN]
• CW032

  Do not use the product after the expiry date shown on the pack [EN]
• CW999

  Dispose of the product according to your local waste management regulations
• CW999

  Keep out of reach of children
• CW275

  Consult your doctor before you use this product if you are pregnant or breast-feeding [EN]
• CW999

  For external use, do not swallow
• CW999

  Do not try to tamper or disassemble the nozzle from the bottle

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

Dénomination commerciale

LUBRI EYES

Code d'UDI-DI

08057729511272

Basic UDI-DI

803395976DT01DT004ZF

Numéro de référence/catalogue

DT/01/DT/004

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

Aucune dimension clinique enregistrée pour ce dispositif.

• 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