These devices do not contain latex.
You must check the product composition to ensure that the patient is not allergic.
Do not use if the packaging is damaged. Connect the infusion set aseptically.
It is essential to check the tightness of the connections with associated medical devices before use.
Dispose of in accordance with Member State regulations.
Contact with 0.5% or 2% Chlorhexidine in 70° Isopropyl alcohol, without evaporation time, and while the luer lock is connected, therefore under physical stress, presents a significant risk of cracking of the luer lock, and should be avoided as much as possible.
In accordance with the recommendations of the SF2H (2019), disinfecting the connectors (when necessary) with 70° ethyl alcohol is always preferable, as it is just as effective in disinfecting inert materials and there is much less risk of altering plastic materials.
Any serious incident must be reported to the manufacturer (materiovigilance@didactic.fr) or to the competent authorities.
For infusion sets with rotary flow regulators (ref: PER1FLPFP & PER1FLPYFP):
Avoid using a flow regulator with solutions that are too viscous to ensure proper control of the infusion rate.
Do not use with: Lipid emulsions, parenteral nutrition bags – Glucose solutions ≥ 20% (G20%, G30%) – Mannitol 20% – Vascular filling solutions, hydroxyethyl starches (such as Voluven 6%, Heafusine 6%, Hesteril 6%) – Blood and blood products.
Do not use with high-risk medications, medications with a narrow therapeutic index (such as catecholamines, morphine, heparin, insulin, potassium chloride, anticancer drugs requiring administration via infusion pump, and any pharmaceutical specialties that specify in their SPC (Summary of Product Characteristics) the need for administration via infusion pump or syringe driver).
