Trekplaister Oordruppels

Nom de l'organisation

SRN

PL-MF-000007178

Statut du fabricant

Actif

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

• Ne pas utiliser si l’emballage est endommagé

  If the packaging has been damaged.

• If the ear drum is damaged (e.g. chronic otitis media); • medical device should only be used after a thorough otoscopic examination by a doctor; • the expiry date printed on the packaging has expired; • the patient is immediately after surgery or surgical treatment in the ear; • in children under 6 months of age; • in case of prolonged pain or swelling caused by inflammatory condition with bacterial or fungal basis, these ailments require contact with a doctor; • in case of ear discharge - leakage from the ear; • medical device should not be applied to the ear with the hearing aid fitted, medical device should be applied one hour before the hearing aid is ingested into the outer ear canal; • although there is no evidence that medical device drops have a negative effect when used during pregnancy and breast-feeding, the use of medical device drops should be consulted with a doctor who should assess whether the expected benefits of it exceed the potential risk; • if symptoms intensify or there is no improvement after three days of using medical device ear drops or if you have a fever, contact your doctor. Prolonged pain or swelling may signal a bacterial or fungal infection that may require further and more appropriate treatment; • for external use only; • avoid contact with eyes, mouth and throat and nose mucous membranes; • It is intended for temporary relief of ear pain, no longer than 3 days and should not be used chronically.

  AUTRE

• EUH 208 - Contient <nom de la substance sensibilisante>. Peut produire une réaction allergique.

  An allergy to any of the components of the product has been previously detected; (Glycerol and lidokaine).

Marché principal en Pologne ; disponible dans 2 pays au total.

• 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.

• M9002PROTECTIVE DEVICES, LUBRICANTS AND SOOTHING DEVICES (SPRAYS, GELS, FLUIDS AND CREAMS)

• Dispositifs médicaux de Classe III dans EUDAMED

Santé des certificats sur le portefeuille de ce fabricant.