BUTIRECT

Nom de l'organisation

SRN

PL-MF-000005402

Statut du fabricant

Actif

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

• The main contraindications: 1.Hypersensitivity to any substance contained in suppositories. 2.Neoplastic changes of the rectum. 3.Severe, sharp pain in the anal area. 4.Bleeding from the rectum, spontaneous or during a bowel movement, understood as bright red blood on the stools. Contraindication 1 was formulated on the basis of a risk analysis at the design stage. Contraindication 2, 3, 4 was formulated on the basis of the knowledge that the clinical conditions listed in these sections require consultation with a physician. In these cases, the medical device rectal suppositories may be used only on an express medical prescription. The product has no influence on the ability to drive and operate machines. Do not use if package is damaged. Do not use the product after the expiry date marked on the packaging. Do not use the product if the packaging is damaged or not tampered with before opening it for the first time. The product is intended for adults. Use the product during pregnancy and breastfeeding only on explicit medical prescription. Do not use while using other rectal products and medications without consulting your doctor. Do not use vaginally. Intended only for rectal use - do not consume.

  AUTRE

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

• 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.

• G05TOPICAL ANORECTAL ADMINISTERED GASTRO-INTESTINAL SYSTEM DEVICES

• Dispositifs médicaux de Classe IIa dans EUDAMED

Aucun certificat ne référence l'IUD-ID de base de ce dispositif.

Santé des certificats sur le portefeuille de ce fabricant.