Abbott ID NOW Instrument – Rapid Molecular Testing for Infectious Diseases

The Abbott ID NOW Instrument is a cutting-edge, rapid molecular testing system designed for fast and accurate detection of infectious diseases at the point of care. Using isothermal nucleic acid amplification technology, the device provides reliable results in under 15 minutes, helping healthcare professionals make faster clinical decisions and improve patient outcomes.

Its compact design and minimal training requirements make the Abbott ID NOW ideal for use in a variety of settings including hospitals, clinics, urgent care centres, and mobile units. The system supports antimicrobial stewardship by enabling timely and appropriate treatment decisions, ultimately reducing healthcare costs and optimising infection control practices.

Key Features & Benefits:

• Ultra-Fast Molecular Results – Get positive results in minutes and final results in under 15 minutes.

• Isothermal Nucleic Acid Amplification – Ensures high sensitivity and specificity in detecting infectious diseases.

• Compact & Portable Design – Small footprint allows for use in hospitals, clinics, and mobile testing units.

• Minimal Training Required – Simple interface for ease of use by healthcare professionals.

• Seamless Connectivity – Results can be integrated with hospital and lab networks for efficient patient management.

• Antimicrobial Stewardship – Supports the appropriate use of antibiotics and antivirals, reducing drug resistance risks.

• Optimises Infection Control – Rapid detection facilitates timely isolation and treatment decisions.

• Reliable Near-Patient Testing – Helps reduce hospital stays and overall healthcare costs.

• Broad Infectious Disease Testing – Detects Influenza A & B, Strep A, RSV, and more.

• FDA, CE, and Health Canada Approved – Trusted by medical institutions worldwide.

Information on this page is provided for guidance and does not replace advice from a qualified clinician. Always read the manufacturer's instructions before use, and check that a device is suitable for the patient and the prescribed therapy.