ITVN10

Nom de l'organisation

Nirial Pharma srl

SRN

IT-MF-000018760

Statut du fabricant

Actif

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

• CW275

  In pregnancy and breastfeeding, consult your doctor first.
• CW010

  EUDAMED n'a pas publié de description pour ce code.
• CW007

  Before the first use, check that the product is properly closed and not damaged.
• CW277

  If you experience any side effects, stop using the product, contact your doctor and inform the manufacturer.
• CW999

  Drug interactions: No drug interactions are known. The use of other ophthalmic product (drugs or medical device) should be done at least 15 minutes after the instillation of this eye spray. The oral administration of other medical devices, drugs or supplements concomitantly with this eye spray should be carried out under the supervision of a doctor. Contraindications: Sensitivity or known allergy to any ingredient. Precautions and warnings: For contact lens wearers: the product should be used between wears. DO NOT SPRAY ON OPEN EYES. In case of direct contact with the open eye, the product may cause a mild burning sensation, which disappears quickly with no after effects. If the burning sensation persists, rinse eyes with plenty of water. Any serious accident occurring in relation to the device must be promptly reported to the manufacturer and the competent authority of the Member State where the user and / or patient is established. Do not use the product in case of hypersensitivity or known allergy to one or more of its ingredients. Keep away from children's sight and reach. The use in children must be supervised by an adult. Product for external use only.

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

Dénomination commerciale

non renseigné

Code d'UDI-DI

08052990632183

Basic UDI-DI

805299063OFTASPRAY001KC

Numéro de référence/catalogue

ITVN10

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