ISO 80369-6 has been developed to address the incidence of accidental misconnections and injections to the patient in neuroaxial applications.
This standard defines new requirements for small bore connectors in medical applications.
Instead of the well established universal LUER connector, each system-specific application has its own unique connector.
NRFit advantages at a glance:
• Increased patient safety
• Unnoticed misconnections are almost impossible
• Clear labelling on products and packaging (with Yellow color coding.)
• A Product offered according to ISO 80369-6 must contain the phrase "NRFit" in its trade name: eg "Sprotte NRFit"
• No loss of functionality or scope or performance in NRFit versions of existing legacy "Luer type" devices
Pajunk NRFit Product Range
• Spinal/Epidural/Combined Spinal-Epidural (CSE)
• Peripheral nerve blocks
• Lumbar puncture
• Wound infiltration
Limited compatibility
The compatibility of the NRFit connectors is limited to the neuroaxial applications defined under ISO 80369-6.
Avoidance of misconnections
The probability of misconnection or misinjection is minimised by the new series of standards.
Is your institution or practise converting to NRFit? The following Webinars guide you through the process ....
Pajunk NRFit Product Range
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