Baxter Announces U.S. FDA Clearance of Novum IQ Syringe Infusion Pump with Dose IQ Safety Software
Baxter International (NYSE:BAX) has received FDA 510(k) clearance for its new Novum IQ syringe infusion pump, which features Dose IQ
- FDA clearance for the Novum IQ syringe infusion pump supports growth in the medication delivery market.
- Dose IQ
Safety Software enhances medication safety, potentially reducing errors in patient care. - Integration with hospital EMRs allows for streamlined processes and better data management.
- None.
- Furthers Baxter’s continued innovation in medication delivery and management
- Integrates Baxter’s decades of leadership in infusion therapy with innovative digital health solutions to build on the company’s proven technology for helping to protect infusions from medication errors
- Supports neonatal and pediatric clinicians and anesthesiologists to help provide safe, accurate infusions for vulnerable patients
Syringe infusion pumps are typically used to precisely deliver small amounts of fluid at low rates, often in pediatric, neonatal or anesthesia care settings. The Novum IQ SYR delivers a technologically integrated user experience with enhanced safety features, advanced connectivity, configurable anesthesia care settings and a robust portfolio of sets designed to help deliver optimum accuracy. Its user interface incorporates features including colored visual banners that clearly identify enteral delivery, a backlit keypad and guided syringe loading.
“We are thrilled to bring a new syringe infusion pump to the market that represents the next generation of Baxter’s intelligent infusion ecosystem,” said
Protecting More Infusions with Advanced Technologies
Advancing the safety and efficiency of medication delivery and management is critical, as data continues to show the harmful burden of errors on patient safety.1,2 The Novum IQ SYR utilizes intuitive technologies built to help reduce infusion errors and was designed to meet rigorous FDA guidance for infusion devices, including cybersecurity.
The Novum IQ SYR features Baxter’s Dose IQ
- Helping ensure pumps are up to date with the latest drug and dose information through centralized access to drug library files
- Incorporating titration error prevention technology to provide additional safety measures for infusions
- Optimizing information technology infrastructure and accessibility
- Offering flexibility to scale as hospital systems and technologies evolve
In addition to fully integrating the Novum IQ SYR with hospital EMRs, Baxter’s IQ Enterprise Connectivity Suite:
- Enables over-the-air operating system upgrades to all Novum IQ SYRs connected to a hospital’s network
- Allows option to enable auto-programming and auto-documentation of infusion data through full bi-directional integration with EMRs
- Delivers near real-time infusion data and streamlined infusion reports
- Provides clear visualizations of infusion data across a hospital system, allowing efficient identification of safety and process issues at every level of care
- Offers option to implement tagless asset tracking that shows infusion pump location and status throughout the hospital, helping to save time and optimize resources
Baxter’s Novum IQ platform, which currently includes the Novum IQ SYR, Dose IQ
For more information on the Novum IQ SYR, please visit Baxter.com.
About Baxter
Every day, millions of patients, caregivers and healthcare providers rely on Baxter’s leading portfolio of diagnostic, critical care, kidney care, nutrition, hospital and surgical products used across patient homes, hospitals, physician offices and other sites of care. For 90 years, we’ve been operating at the critical intersection where innovations that save and sustain lives meet the healthcare providers who make it happen. With products, digital health solutions and therapies available in more than 100 countries, Baxter’s employees worldwide are now building upon the company’s rich heritage of medical breakthroughs to advance the next generation of transformative healthcare innovations. To learn more, visit www.baxter.com and follow us on Twitter, LinkedIn and Facebook.
Novum IQ SYR Indications for Use
The Novum IQ syringe pump is intended to be used for the controlled administration of fluids. These include pharmaceutical drugs, parenteral nutrition, blood and blood products, and enteral nutrition. The Novum IQ syringe pump is intended to deliver an infusion through the following clinically accepted routes of administration: intravenous, arterial, enteral, and subcutaneous. The Novum IQ syringe pump is intended to be used in conjunction with legally marketed and compatible administration sets, syringes, and medications provided by the user. The Novum IQ syringe pump is suitable for patient care in hospitals and outpatient health care facilities. The Novum IQ syringe pump is intended for use on adults, pediatrics and neonates.
The Novum IQ syringe pump is intended to aid in the reduction of operator interaction through guided programming, including a way to automate the programming of infusion parameters and documentation of infusion therapies when integrated with an Electronic Medical Record (EMR) system. This automation is intended to aid in the reduction of programming errors. The Novum IQ syringe pump is intended to be used by trained healthcare professionals.
Dose IQ Safety Software Intended Use
Dose IQ
Rx only. For safe and proper use of the products mentioned herein, please refer to the appropriate Operators Manual or Instructions for Use.
This release includes forward-looking statements concerning the Novum IQ syringe pump, Dose IQ and IQ Enterprise, including potential benefits associated with their use and statements regarding future anticipated launches of the Novum IQ platform. The statements are based on assumptions about many important factors, including the following, which could cause actual results to differ materially from those in the forward-looking statements: demand for and market acceptance for new and existing products; product development risks; inability to create additional production capacity in a timely manner or the occurrence of other manufacturing or supply difficulties (including as a result of natural disasters, public health crises and epidemics/pandemics, regulatory actions or otherwise); satisfaction of regulatory and other requirements; actions of regulatory bodies and other governmental authorities; product quality, manufacturing or supply, or patient safety issues; changes in law and regulations; and other risks identified in Baxter's most recent filings on Form 10-K, Form 10-Q and other
Baxter, Novum IQ, Dose IQ and IQ Enterprise are registered trademarks of
1 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5770837/pdf/bmjopen-2017-015912.pdf
2 https://www.fda.gov/drugs/drug-information-consumers/working-reduce-medication-errors
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