BIOpH+ Medical foot bath

Nom de l'organisation

Biocool AB

SRN

SE-MF-000012411

Statut du fabricant

Actif

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

• CW010

  Read the instructions and warnings before use. Keep sealed, out of reach of children, at room temperature and away from inflammable substances. Avoid contact with eyes; in the event of contact with eyes, rinse with water for at least 10 minutes. In case of medical concern consult health care proffessional. For external use. Avoid contact with open wounds. Diabetics: Pay special attention to skin damage and consult a healthcare provider if unsure. Check skin regularly during use. Redness or irritation may occur without being felt due to reduced sensation. Diabetics: Consult your healthcare provider before use. Check skin regularly during use. Inspect feet before treatment; do not use on open wounds or infections. Stop treatment if symptoms worsen. Redness or irritation may occur without being felt due to reduced sensation. After use, dry feet carefully, especially between toes (important for diabetic patients). If needed, apply moisturizer after treatment, but avoid between toes to reduce risk of skin damage.

Marché principal en Suède ; disponible dans 5 pays au total.

Dénomination commerciale

BIOpH+ Medical foot bath

Code d'UDI-DI

07392059101726

Basic UDI-DI

739205910BPPFCCA

Numéro de référence/catalogue

1000008

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

Medical treatment that alleviates the symptoms associated with foot fungus (erythema, erosions, macerations, pruritus, fissures, burning/stinging, hyperkeratosis, and odour), heel cracks and calluses. SUITABLE FOR DIABETICS MULTIFUNCTIONAL TREATMENT CLINICALLY PROVEN TO TREAT ATHLETE'S FOOT GENTLE EXFOLIATION IMPROVES SKIN BARRIER

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.

• V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER

Santé des certificats sur le portefeuille de ce fabricant.