The Masimo NomoLine-O LH Airway Adapter Set (2m) is a high-performance capnography sampling line designed for accurate end-tidal CO2 (EtCO2) monitoring in EMS, hospital, and critical care environments. Engineered with Masimo’s advanced moisture management technology, this airway adapter ensures reliable gas sampling even in high-humidity and demanding clinical conditions.
Designed for intubated patients, this low-humidity (LH) sampling line features integrated tubing, an airway adapter, and a hydrophobic filter to help reduce contamination and maintain consistent CO2 readings. It is a critical component for any advanced respiratory monitoring setup.
Key Features
Masimo NomoLine-O LH airway adapter set (2m length)
Designed for EtCO2 capnography monitoring
Compatible with ZOLL X Series and Propaq MD systems
Moisture-wicking technology for reliable performance
Hydrophobic filter reduces contamination risk
Low dead space design for fast and accurate response
Single-use for infection control and patient safety
Available Options
Single unit (individually packaged)
Box of 10 (bulk packaging for high-volume use)
Applications
Emergency Medical Services (EMS)
Hospitals and critical care units
Intubated patient monitoring
Capnography and respiratory monitoring
Condition
New, single-use airway adapter sets. Ready for immediate clinical use.
👉 Contact us for bulk pricing, case quantities, and complete capnography system packages.
Masimo NomoLine-O LH Airway Adapter 2m | ZOLL X Series EtCO2
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Refurbished Equipment Disclaimer
Some equipment offered by Parrott Med is refurbished. Refurbished devices are inspected and tested to help ensure proper functionality; however, they may not be certified by the original manufacturer unless explicitly stated.
Parrott Med is an independent reseller and is not aAiliated with or authorized by all original equipment manufacturers unless otherwise specified.
FDA / Regulatory Disclaimer
Certain medical devices sold by Parrott Med may be subject to regulation by the U.S. Food and Drug Administration (FDA). It is the responsibility of the purchaser to ensure compliance with all applicable regulatory requirements, including device registration, use, and maintenance.
Parrott Med does not provide medical or regulatory advice. Buyers should consult appropriate regulatory authorities or qualified professionals regarding compliance requirements.
Limitation of Liability
All equipment is sold in accordance with the terms outlined at the time of sale. Parrott Med shall not be held liable for improper use, installation, or operation of any equipment after delivery.
Buyers are responsible for ensuring that all equipment is properly installed, maintained, and operated by qualified personnel.
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