DayDrop 20ud x 0.4ml

Nom de l'organisation

i+Med S.Coop.

SRN

ES-MF-000008633

Statut du fabricant

Actif

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• CW010

  EUDAMED n'a pas publié de description pour ce code.
• CW009

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

  EUDAMED n'a pas publié de description pour ce code.
• CW032

  Do not use the product after the expiration date indicated on the box or on the packaging.
• CW277

  Contact your doctor or pharmacist if you notice any side effects related to using DAYDROP. lf these effects persist or worsen, consult your doctor or pharmacist.
• CW135

  Keep out of the sight and reach of children. Use with caution in pediatric population (product not evaluated in children).
• CW276

  Do not use with other products containing quaternary ammonium salts such as benzalkonium chloride because sodium hyaluronate may precipitate in its presence. After using DAYDROP, wait at least 15 minutes to apply any other product or medicine to the eye. DAYDROP is compatible with contact lenses . After putting on the contact lenses and before applying the drops, it is recommended to wait about 30 minutes to avoid incompatibility reactions between the products used for the maintenance of contact lenses and DAYDROP.
• CW999

  Do not administer DAYDROP if you have hypersensitivity to hyaluronic acid or other components of the product. Do not use if you are allergic to any ingredient. Do not touch your eye, or any surface with the tip of the product vial. Do not share the product with other people. May cause temporary blurring immediately after using the drops. Wait for clear vision before carrying out risky activities. For external use only, do not ingest.
• CW275

  Consult your doctor, pharmacist or optician before using the product during pregnancy or breast-feeding.

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

Dénomination commerciale

DayDrop 20ud x 0.4ml

Code d'UDI-DI

08437015992174

Basic UDI-DI

B-08437015992174

Numéro de référence/catalogue

PV00047

Entité d'attribution

GS1

Catégorie de risque

Classe IIa

Législation applicable

MDD [Directive 93/42/CEE relative 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.

• Q02030206EYE LUBRICANT SOLUTIONS

• Numéro de lot
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