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This device doesn’t contain latex.
You should check the composition of product to ensure that the patient isn’t allergic.
Do not use if 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 according to the regulations of the member states.
Prolonged contact with 2% Chlorhexidine/70° Isopropyl Alcohol without an evaporation time, while the Luer Lock is connected and under physical stress, presents a significant risk of Luer Lock cracking and should be avoided as much as possible.
In accordance with the current SF2H recommendations, disinfection of connectors (when necessary) with 70° ethyl alcohol is always preferable, as it is just as effective for disinfecting inert materials and carries a much lower risk of plastic degradation.
Any serious incident must be reported to the manufacturer (materiovigilance@didactic.fret/or to the competent authorities).
For the IV Infusion set with rotative flow regulator (ref: PER1FLPFP & PER1FLPYFP)
Avoid using a flow regulator with solutions that are too viscous to allow good control of the infusion rate. Do not use with: Lipid emulsions, parenteral nutrition pockets – Carbohydrate solutions ≥ 20% (G20%, G30%) – Mannitol 20% – Vascular filler solutions, hydroxyethyl starches (type Voluven 6%, Heafusine 6%, Hesteril 6%) – Blood and blood derivatives
Do not use with high-risk drugs, drugs with a narrow therapeutic margin (for example catecholamines, morphines, heparin, insulin, potassium chloride, anticancer requiring administration by infusion pump, and all pharmaceutical specialties which include in the R.C.P. the need for administration by infusion pump or syringe pump. )