SLBCRVN50

Nom de l'organisation

Nirial Pharma srl

SRN

IT-MF-000018760

Statut du fabricant

Actif

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

• CW275

  Consult your doctor or pharmacist before using the product in pregnant, breastfeeding women and in children under 3 years old.
• CW010

  EUDAMED n'a pas publié de description pour ce code.
• CW007

  Do not use if the tube is open or damaged.
• CW135

  EUDAMED n'a pas publié de description pour ce code.
• CW999

  Any adverse event or serious accident occurring during use of the device must be promptly reported to the manufacturer identified on the product and in the instructions for use.
• CW999

  If any adverse reactions occur or an allergy to any of the ingredients emerges, the treatment should be discontinued.
• CW999

  Do not swallow. Avoid contact with your eyes; in case of contact, rinse immediately with plenty of water.
• CW999

  The use of the formulation can occasionally cause transient irritation. This is the only foreseeable side effects of the device, moreover it would be occasional and transient, without need of countermeasure.
• CW999

  Do not use in conjunction with other therapies or treatments in place that involve taking or topical use of other medical devices, drugs or supplements.
• CW999

  Any serious accident occurring in relation to the device must be promptly reported to the manufacturer and the competent authority of the Member State where the user and / or patient is established.
• CW999

  Do not rub the cream into the treated area after application. It is advisable to protect the medicated part with a sterile gauze.
• CW999

  Keep the package leaflet close at hand so that it can be consulted should the need arise.
• CW999

  Close the tube well after use.
• CW999

  Avoid direct contact between the tube and the lesion.
• CW999

  The product should be used by one person only so as to avoid the risk of cross contamination.

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

Dénomination commerciale

non renseigné

Code d'UDI-DI

08052990630820

Basic UDI-DI

805299063DERMA001UC

Numéro de référence/catalogue

SLBCRVN50

Entité d'attribution

GS1

Catégorie de risque

Classe IIa

Législation applicable

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

Statut

Sur le marché

Quantité

1

Description complémentaire du produit

—

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.

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