PACTRYS-NCA



  • The choice of interface affects the efficacy of NIV.

 

  • The pressures as measured by the ventilators (before the interface) are dependent on interface resistence are not equivalent to what is delivered to the lung

 

  • Evaluation of a nasal cannula in noninvasive ventilation using a lung simulator. Iyer NP, Chatburn R.Respir Care. 2015 Apr;60(4):508-12.

 

  • Neonatal nasal intermittent positive pressure ventilation efficacy and lung pressure transmission. Mukerji A, Belik J.J Perinatol. 2015 Sep;35(9):716-9.

 

  • Tidal volume transmission during non-synchronized nasal intermittent positive pressure ventilation via RAM(®) cannula. Matlock DN, Bai S, Weisner MD, Comtois N, Beck J, Sinderby C, Courtney SE.J Perinatol. 2019 May;39(5):723-729.

SIZES :

NASALCANNULAØ2-L8mm with CPAP Holder & 25 cm Bonnet

NASALCANNULAØ2-L10mm with CPAP Holder & 25 cm Bonnet

NASALCANNULAØ3-L12mmwith CPAP Holder & 30 cm Bonnet

NASALCANNULAØ4-L14mmwith CPAP Holder & 35 cm Bonnet

 

INDICATIONS FOR USE

The PACTRYS®-NCA is a product intended for use on premature and newborn babies that require supplemental oxygen, respiratory support or assistance in breathing in an outpatient, hospital or institutional setting.

It is used for Non-invasive ventilation

INSTRUCTIONS FOR USE

Select an appropriately sized cannula.

Non Invasive Ventilation:

  • For non-invasive ventilation (NIV) the cannulas must adhere completely to the wall of the nostrils so as it is snuggly fitted in nostrils.
  • Connect CPAP Bubble Holder Set with Cannula & fix assembly with Bonnet.
  • Connect the Bubble Holder set with gas source, making sure that all the connections are properly secured
  • Open and test the gas flow level before placing the device on the patient.
  • Insert the cannula into the patient’s nostrils and leave a small gap between the patient’s septum and the base of the cannulas.
  • Replace the PACTRYS®-NCA every 7 days or according to the hospital protocol, whichever occurs first. Dispose of the used PACTRYS®-NCA according to hospital protocol.

 TECHNICAL CHARACTERISTICS

  • Soft and delicate interface
  • Individually packaged
  • Single use
  • Made of high performance TPE suitable for medical use
  • Connection: M15mm
  • Dimensions: 4 sizes XXS, XS, S, M
  • Class according to 93/42 EEC directive: IIa

      

Components of NASAL CANNULA ACCESSORIES

Nasal Cannula

Bonnet made up of 100% cotton with elasticity

Bubble CPAP Cannula Holder Set includes :

Y Connector With Water Condensation Line out

White Cap

Two Expandable Tubes (upto 70 cm-Ø10 F)


WARNINGS

•       This device must be used only when the patient is under the continuous and direct supervision of the healthcare professional and frequent observation of the position of the cannula in the patient’s nostrils is necessary.

•       Incorrect choice of size, improper placement or use can cause septal trauma or necrosis.

•       The cannula tubes can represent a potential strangulation hazard.

•       Always start the gas flow before inserting the cannula into the patient’s nostrils.

•       Do not use if the package is damaged or opened.

•       Do not immerse, wash or sterilize.

•       Stop immediately if skin irritation occurs.

•       For single patient use only.

•       The device must be stored in a suitable, cool and dry place away from heat sources.

•       Avoid exposure to direct light sources.

•       The product, if it comes into contact with it, has chemical-physical incompatibilities with organic solvents (petrol, benzoyl, esters, ketones, chlorine hydrocarbon).

TYPE SIZE OUTER DIAMETER(mm) PRONGS LENGTH (mm) BONNET SIZE
NASAL CANNULA XXS 2 8 25 cm
NASAL CANNULA XS 2 10 25 cm
NASAL CANNULA S 3 12 30 cm
NASAL CANNULA M 4 14 35 cm