ZOLL NIBP Hose 8300-0002-01 | X Series & Propaq MD Blood Pressure Tubing
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SKU: 8300-0002-01

ZOLL NIBP Hose 8300-0002-01 | X Series & Propaq MD Blood Pressure Tubing
$0.00 USD $0.00 USD
In stock
Description

Product Description 

The ZOLL X Series & Propaq MD NIBP Hose (8300-0002-01) is a dual-lumen blood pressure tubing assembly designed for accurate non-invasive blood pressure monitoring in EMS and clinical environments. Compatible with ZOLL X Series and Propaq MD monitor defibrillators, this hose connects the monitor to the NIBP cuff system to deliver reliable and consistent readings.

Engineered for durability and performance, this 10-foot dual-lumen hose allows for flexibility during patient care while maintaining accurate pressure transmission. It is an essential component for any complete monitoring setup used in emergency response, transport, and hospital settings.

Key Features

  • OEM ZOLL dual-lumen NIBP hose (8300-0002-01)
  • Compatible with ZOLL X Series and Propaq MD devices
  • 10-foot tubing length for flexibility in patient care
  • Dual-lumen design for accurate pressure monitoring
  • Secure connectors for reliable attachment
  • Built for EMS, hospital, and transport environments

Applications

  • Emergency Medical Services (EMS)
  • Hospitals and emergency departments
  • Ambulance and transport teams
  • Routine and critical patient monitoring

Condition

Available new or refurbished. Fully tested and ready for use.

👉 Contact us for bundle options including NIBP cuffs, monitors, and full system configurations.

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.