ELANEE Vaginal-Ovula

Nom de l'organisation

SRN

PL-MF-000005402

Statut du fabricant

Actif

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

• CW275

  During pregnancy and breastfeeding, use only after consulting a doctor or pharmacist.
• CW007

  Do not use if the packaging is damaged
• CW129

  When using the product in cases of severe vaginal dryness, due to the lactic acid content of the product, slight reactions may occur at the site of application (mild burning or itching). These symptoms are temporary and usually disappear spontaneously. If the symptoms persist, this may indicate hypersensitivity to the ingredients of the product. In this case, discontinue use and consult your doctor or pharmacist.
• CW277

  If vaginal dryness persists, consult your doctor or pharmacist.
• CW160

  Avoid accidental contact of the product with the mucous membranes of the eyes, nose or mouth.
• CW149

  Store the product in its original packaging.
• CW999

  Hypersensitivity to the product components / occurrence of adverse reactions after use of the product: - Do not use the product if you are hypersensitive (allergic) to any of its ingredients. - If the patient has no known hypersensitivity to the ingredients of the product and during use of the product a burning sensation, itching or redness appears which does not subside spontaneously, this may indicate hypersensitivity to the ingredients of the product, in which case you should discontinue use of the product and consult your doctor or pharmacist. Do not use with local anaesthetics or other vaginal preparations, as the product may weaken or delay their action. Do not use with latex condoms and contraceptive inserts, as the product may reduce their effectiveness due to its fat content. Do not have sexual intercourse immediately after applying the suppository. The product can be used with other vaginal products if recommended by a doctor. Do not use during menstruation. The product is intended for vaginal use only. Do not reuse a suppository once it has been inserted.

Marché principal en Allemagne ; disponible dans 3 pays au total.

• Numéro de lot
• Date d'expiration
• Date de fabrication
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• Identification du logiciel

Nomenclature européenne des dispositifs médicaux — la classification produit UE attribuée à ce dispositif.

• U089005PESSARIANS

• Dispositifs médicaux de Classe IIb dans EUDAMED

Aucun certificat ne référence l'IUD-ID de base de ce dispositif.