FTP096

Dénomination commerciale

non renseigné

Code d'IUD-ID

D-FTP096_3L7

IUD-ID de base

B-FTP096_3L7

Numéro de référence/catalogue

FTP096

Entité d'attribution

EUDAMED

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

FILMATUSS SCIROPPO IN BUSTINE is a medical device designed for the treatment of dry and wet cough and sore throat.

URL des informations complémentaires

Aucune URL d'informations complémentaires renseignée par le fabricant.

Dimensions cliniques

Aucune dimension clinique enregistrée pour ce dispositif.

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

• V9017ORAL ADMINISTRATION PREPARATIONS NOT INCLUDED IN OTHER CLASSES

1 avertissement enregistré — faire défiler le panneau pour tout voir.

• CW999

  - Do not take it if you are allergic or hypersensitive to any component. - Do not use the product after the expiry date printed on the package. - Keep out of children's reach. - Shake the stick pack (or bottle) before use. - Wash carefully the measuring cup after use (bottle package only) - Close the bottle accurately after use (bottle package only) - The period of validity after the first opening of the syrup is 3 months (12 weeks) [bottle package only] - Do not use in case the packaging is not intact or damaged; - The syrup has been specifically dosed for children from 3 years old, do not administer to children under 3 years of age. - If you do not notice appreciable results after a short period of treatment (7 days), contact your doctor; in any case do not use for more than 15 days. - So far, no side effects have been observed as a result of the administration of the device. However, if you notice the appearance of side effects, inform your doctor or pharmacist. - The expiry date refers to the packaged product intact, properly stored. - Once the stick pack has been opened, use all its content (stick pack package only)

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