BUTYNORM

Nom de l'organisation

LABORATOIRE L'IDEAL Parisien Sp. z o.o.

SRN

PL-MF-000005402

Statut du fabricant

Actif

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

• CW999

  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.

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

Dénomination commerciale

BUTYNORM

Code d'UDI-DI

05906122471207

Basic UDI-DI

B-05906122471207

Numéro de référence/catalogue

BUTYNORM Rectal suppositories, 10 suppositories in carton with instructions for use. Language version: Ukrainian

Entité d'attribution

GS1

Catégorie de risque

Classe IIa

Législation applicable

MDD [Directive 93/42/CEE relative aux dispositifs médicaux]

Statut

Sur le marché

Quantité

1

Description complémentaire du produit

Medical device intended for rectal use. A suppository inserted into the anal canal, after contact with the mucus produced physiologically by the goblet cells of the rectal mucosa, creates a protective coating on the mucosa surface with mucoadhesive properties. This protects and improves the hydration of the rectal mucosa. Intended for rectal use in order to: restore the natural physiological state of the rectal mucosa, support the regeneration of erosions, cracks or other defects in the rectal mucosa, alleviation of painful symptoms of emptying associated with damage to the epithelium or the presence of an inflammatory process in the rectum, supporting the regeneration of anal canal tissues after surgery or radiotherapy.

URL des informations complémentaires

https://www.lideal.pl/

Dimensions cliniques

• 2 MU24

• 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