GRANIONS® SPRAY GORGE FR

Nom de l'organisation

Labomar S.p.A.

SRN

IT-MF-000007965

Statut du fabricant

Actif

Santé des certificats sur le portefeuille de ce fabricant.

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

• CW999

  - Do not take if hypersensitive or allergic to one of the components: - Do not use the product after the expiration date on the package; - Keep out of children's reach; - Shake the vial before use; - The period of validity after the first use is 3 months (12 weeks); - The use of the same vial by several subjects can facilitate the transmission of infections: strictly personal use of the product is recommended; - Wash and dry carefully the dispenser before and after use; - Do not use in case the packaging is not intact; - 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.

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

Dénomination commerciale

GRANIONS® SPRAY GORGE FR

Code d'UDI-DI

D-FTP098FG

Basic UDI-DI

B-FTP098FG

Numéro de référence/catalogue

FTP098

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

GRANIONS® SPRAY GORGE is a medical device composed of substances, non-sterile, intended for short term invasive contact with respect to body orifices (oral cavity), designed for the treatment of dry and wet cough and sore throat. Gorgewell spray intended for adult and children above 3 years of age.

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