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CADD® and Portex® Portfolio with the NRFit™ Connector

Secure Connections from Pump to Patient

  Aware

 In 2014, the Joint Commission released Sentinel Event Alert 53: Managing Risk During Transition to ISO Tubing Connector Standards. The ISO 80369-6 neuraxial connector standard was published on March 2016. The goal is to reduce the incidence of medical device misconnections by creating unique non-Luer connectors for neuraxial procedures. The neuraxial non-Luer connectors will be branded by all major manufacturers as NRFit® connectors.

  Prepare

 Smiths Medical would like to help you with switching to the NRFit® neuraxial non-Luer connector. We’ll help make the transition easier by providing support, guidance and product expertise.

  Adopt

 Before your facility adopts the new standard, it is important that all employees who will be involved become educated on the new 80369-6 standard for proper use of non-Luer connectors. Share the information with your entire team, and be sure everyone understands the importance of this change.


Additional Information

 

StayConnected.org

Sentinel Event Alert 53: Managing Risk During Transition to ISO Tubing Connector Standards

FDA: Reducing Risks through Standards Development for Medical Device Connectors

NRFit - New ISO Standard

Security From Pump To Patient

A COMPLETE NEURAXIAL SOLUTION THAT PROMOTES PATIENT SECURITY

The CADD® and Portex® Portfolio with the NRFit® connector is an ISO 80369-6 compliant connection system intended to enhance patient safety through a reduction in the risk of misconnection, while minimizing any change to clinical technique.

Connections in a snap with the
EpiFuse® catheter connector

The feel of precision from the
Portex® L.O.R. syringe

Free-flow protection with a flip on
CADD™ medication cassette reservoirs

Efficient workflow with
Portex® epidural trays

CADD® AND PORTEX® PORTFOLIO WITH THE NRFIT™ CONNECTOR

COMPLETE SOLUTIONS FOR CONTINUOUS EPIDURAL, SPINAL AND CSE INFUSION PROCEDURES

A TRUSTED BUSINESS PARTNER

Smiths Medical, the developer and manufacturer of the CADD® and Portex® products with the NRFit® connector, is an experienced supplier of specialty medical devices and equipment. The CADD® and Portex® brands of pain management and regional anesthesia products are sold worldwide and have earned a reputation for quality, innovation and performance.


 

Please see the Instructions for Use for a complete listing of the indications, contraindications, warnings and precautions.

Find out more

To find out more about CADD® and Portex® NRFit™ solutions, please fill out the form below.

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