BLAU_PROTECT

Nom de l'organisation

Synkotech Biocompatible Materials S.L

SRN

ES-MF-000031010

Statut du fabricant

Actif

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

• CW010

  If BlauProtect® Advanced comes into contact with the eye, rinse immediately with warm water. Do not rub or attempt to separate the eyelids. Seek medical attention. • The product is individually packaged and should be discarded after use. Some treatment sites may require the use of more than one unit. • If irritation or prolonged pain develops (redness, swelling, prolonged heat, and change in skin color), discontinue product use immediately. If irritation persists, seek medical attention. • The polymerization of BlauProtect® Advanced may be accelerated in the presence of water or liquids containing alcohol. BlauProtect® Advanced should not be applied to wet or moist skin. • Do not use under medication patches. • Avoid contact with mucous membranes such as eyes and mouth.• BlauProtect® Advanced must dry before coming into contact with other skin or materials to prevent unintended adhesions. • BlauProtect® Advanced may produce a temporary warmth sensation when applied in a thin layer. Excessive application in a thick layer will result in an increase in the warmth intensity. • The use of other barrier products, ointments, creams, or lotions may significantly reduce the product's effectiveness. • Keep out of reach of children. • If BlauProtect® Advanced accidentally comes into contact with an open wound, rinse with warm water. Removal is not necessary. • If the skin or other materials adhere to the area, gently roll to separate them. If unable to separate easily, seek medical attention.
• CW009

  Do not re-use
• CW007

  Do not use if package is damaged
• CW135

  Keep out of reach of children.

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

Dénomination commerciale

non renseigné

Code d'UDI-DI

08437025406845

Basic UDI-DI

8437025406BPG6

Numéro de référence/catalogue

BLAU_PROTECT

Entité d'attribution

GS1

Catégorie de risque

Classe I

Législation applicable

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

Statut

Sur le marché

Quantité

1

Description complémentaire du produit

Advanced Film Barrière Cutané

URL des informations complémentaires

https://synkotechbio.com/es/

Dimensions cliniques

Aucune dimension clinique enregistrée pour ce dispositif.

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

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