SM000012B

Dénomination commerciale

non renseigné

03700512905622

037005129INF-ESTT

Numéro de référence/catalogue

SM000012B

GS1

Classe IIa

Législation applicable

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

Statut

Sur le marché

Quantité

1

Description complémentaire du produit

The Infusion lines cover single use devices, designed for a use from limited use to short-term use. Promepla Infusion lines are intended for use in the administration of intravenous or subcutaneous fluids or as accessories, especially to be used during hemodialysis procedures (performed with hemodialysis central venous catheter access). The Infusion lines family are divided into three categories. The medical devices intended for the intravenous administration are intended to be connected on one side to peripheral intravenous cannulas or needles which are inserted into a vein and a pressure infusion machine on the other side for most cases or syringes/fluids bags. The medical devices intended for the subcutaneous administration are intended to be connected on one side to peripheral subcutaneous invasive device and a pressure infusion machine on the other side for most cases or syringes/fluids bags. The lines can also be completed by a clamp to activate or interrupt fluid circulation. The medical device intended to be an accessory are intended to ensure connection between the hemodialysis central venous catheter (CVC) of a patient and the bloodlines or other extension lines connected to a hemodialyzer or a needleless syringe

URL des informations complémentaires

Aucune URL d'informations complémentaires renseignée par le fabricant.

Dimensions cliniques

Aucune dimension clinique enregistrée pour ce dispositif.

Nomenclature européenne des dispositifs médicaux — la classification produit UE attribuée à ce dispositif.

• A03040199INFUSION KITS (WITH OR W/O PUMP), SINGLE-USE - OTHER