• Pack Components: Includes a 1.1 m heated inspiratory limb, 0.3 m incubator extension, 1.6 m heated expiratory tube with Evaquatechnology, 0.6 m humidifier connection tube with nitric oxide port, swivel wye-piece, MR290V autofeed humidification chamber, pressure line, Dräger adaptors, and label kit change out.
• Materials: Made from polypropylene, polycarbonate, thermoplastic elastomer, various polyethylene types, polyether ester elastomer, silicone, nylon, brass, styrene resin, cyanoacrylate, and DEHP-free PVC. Not made with natural rubber latex.
• Quantity: 10 circuits per carton.
• Carton Dimensions and Weight: 530 mm x 210 mm x 400 mm, weighing 3.99 kg.
• Carton Material: Cardboard box.
• Manufacturing Mode: Produced in a controlled working environment.
• Disposal: Incineration or according to hospital protocol.

• Resistance to Flow: Inspiratory limb - 0.09 ± 0.04 cmH₂O; Expiratory limb - 0.07 ± 0.04 cmH₂O @ 2.5 L/min.
• Flow Rate: 4 - 15 L/min.
• Circuit Length: Both inspiratory and expiratory limbs are 1.6 m.
• Minimum Tube Internal Diameter: 10.2 mm.
• Ambient Range: 20-26 °C / 68-79 °F.
• Compliance: 1.30 ± 0.15 mL/cmH₂O @ 60 cmH₂O.
• Humidifier Compatibility: MR850 humidifier, invasive mode.
• Compressible Volume: 758 mL.
• Duration of Use: 7 days, single patient use.
• Recommended Gas Source: Air/Oxygen.
• Interface Connections: ISO 5356-1 Conical Connectors.
• Shelf Life: 5 years.
• Gas Leakage: <30 mL/min @ 60 cmH₂O.
• Storage Temperature: -10 °C to 50 °C.
• Tidal Volume: <185 mL.

• Interface Connections: ISO 5356-1 Conical connector (22 mm Male).
• Maximum Chamber Operating Pressure: 8 kPa.
• Maximum Peak Flow: 180 L/min for 30 secs.
• Gas Leakage: < 10 mL/min @ 8 kPa.
• Materials: ABS, Polystyrene, Polyethylene, Thermoplastic Elastomer, Aluminium, Ink, Polypropylene, Adhesive, Polycarbonate, Silicone, DEHP-free PVC.
• Compliance: 0.4 mL/cmH₂O.
• Compressible Volume: 280 mL.
• Resistance to Flow: At 60 L/min: 0.52 cmH₂O.

• Classification: AU IIa; EU IIa; CA II; USA II.
• Country of Origin: New Zealand or Mexico.
• Intended Use: For delivering respiratory gases to infant patients dependent on mechanical respiratory support.
• Notified Body Identification Number: TÜV SÜD Product Services GmBH CE0123.
• GTIN Number: 09420012430205 (EA), 09420012424365 (PAC).
• UNSPSC Number: 42272224.
• GDMN Code: 37706.
• Biocompatibility: Meets standards ISO 10993-3, ISO 10993-5, ISO 10993-6, ISO 10993-10.

Evaqua and F&P are trademarks of Fisher & Paykel Healthcare Limited.