FT.MDR.26.100

Nom de l'organisation

GRUPPO FARMAIMPRESA SRL

SRN

IT-MF-000012625

Statut du fabricant

Actif

Santé des certificats sur le portefeuille de ce fabricant.

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

• CW999

  The device is not subject to special precautions of use, we note, however: - Do not use the product more than 30 days - The product may appear with two separate phases. After stirring the same should appear as a homogeneous emulsion. - Keep out of reach of children. - Do not exceed recommended dose. - Do not use after the expiration date, the expiry date refers to the product intact and properly stored. - Do not use if package is not intact. - All the components that make up the product including the dropper must be intact. - After a short period of treatment (7 days) with no significant results, consult a doctor - In case of adverse reactions suspend the use of the product and consult your doctor to fix a proper therapy. - During use, if you find the dropper dirty, clean it properly before inserting it into the bottle to prevent possible contamination. - Do not use in cases of suspected intestinal or ileus perforation. Compliance whit the instructions contained in the leaflet reduces the risk of side effects. It is important to inform your doctor or pharmacist about any side effects not listed in this insert leaflet. In case of a serious accident occurring in relation to the medical device report the incident to the Manufacturer and the Competent Authority.

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

Dénomination commerciale

non renseigné

Code d'UDI-DI

08055748843480

Basic UDI-DI

805574884FTCE16-267U

Numéro de référence/catalogue

FT.MDR.26.100

Entité d'attribution

GS1

Catégorie de risque

Classe IIb

Législation applicable

MDR [Règlement (UE) 2017/745 relatif aux dispositifs médicaux]

Statut

Sur le marché

Quantité

1

Description complémentaire du produit

RILEFAST CE è un dispositivo medico indicato nel trattamento in caso di: Disordini dispeptici, Meteorismo gastroenterico, Aerofagia e Coliche gassose nei lattanti, bambini e adulti.

URL des informations complémentaires

Aucune URL d'informations complémentaires renseignée par le fabricant.

Dimensions cliniques

Aucune dimension clinique enregistrée pour ce dispositif.

• 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.

• G99GASTROINTESTINAL DEVICES - OTHER