2006

Nom de l'organisation

FARMA-DERMA S.r.l.

SRN

IT-MF-000020737

Statut du fabricant

Actif

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

• CW007

  Do not use after the expiry date or if the pack is open or damaged.
• CW010

  Directions for use and warnings: read the instructions for use included in the inside package insert.
• CW135

  Keep out of the reach of children.
• CW999

  CONTRAINDICATIONS Do not use in case of individual hypersensitivity to one of the components of the product.
• CW275

  In caso di gravidanza o allattamento, non essendo stati effettuati studi clinici specifici, consultare il medico prima dell’utilizzo del dispositivo./In case of pregnancy and breastfeeding it is advisable to consult your doctor.
• CW999

  INTERACTIONS WITH OTHER PRODUCTS Interactions with other products are not known, therefore it is advisable to consult the doctor before using PROKTIS-M PLUS rectal ointment in association with other medical devices or drugs for rectal use.
• CW999

  UNDESIRED EFFECTS Use of all products for topical use, especially if prolonged, may cause sensitisation. In that case, or if other undesired effects occur, stop treatment and consult your doctor or pharmacist.
• CW999

  Avoid contact with eyes. Do not swallow.
• CW999

  A personal use of the medical device is recommended. If necessary PROKTIS-M PLUS rectal ointment can be used for prolonged periods, in any case after 30 days of continuous use suspend treatment for one week.

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

Dénomination commerciale

non renseigné

Code d'IUD-ID

08032595871361

IUD-ID de base

803259587TF06EM

Numéro de référence/catalogue

2006

Entité d'attribution

GS1

Catégorie de risque

Classe IIb

Législation applicable

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

Statut

Sur le marché

Quantité

1

Description complémentaire du produit

Indications: adjuvant treatment of reparative processes of the ano-rectal canal following proctological surgery; internal and external haemorrhoids; proctitis; cryptitis; anal rhagades; fissures; perianal fistulae.

URL des informations complémentaires

Aucune URL d'informations complémentaires renseignée par le fabricant.

Dimensions cliniques

• acido ialuronico sale sodico — 0.1 MU999
• white vaseline and vaseline oil — 953 MU999
• Adulti e bambini/Adults and children

• 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