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ensure the safety of your employees and patients wITh superior cstd technology

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Employee safety and patient safety cannot be separated.
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To judge the quality and value of the Q-FLO™ technology, you can study the features and benefits, study the marketing materials, look at the standards it meets and exceeds, and review the Infusion Innovations team behind it all.

But the most important validation of the value of the product comes from customers. 

The following short video shares a customer's viewpoint as he explains why the Q-FLO™ connector is a game-changer. 
"What we love about Q-FLO!"
We switched to Q-FLO for all our Closed System Transfer Devices about 10 weeks ago to compound and administer hazardous drugs at our busy 20-chair facility.

We love the ease of use, the audible and visual confirmation when the device opens or closes.

We were experiencing regular detachment of the previous products we used, which created considerable concern amongst both clients' nurses technicians and our pharmacy staff.

We are fully committed to USP 797 and USP 800. Our absolute priority is the safety of our staff and our patients. Q-FLO provides this comfort.

We have had no detachments or potential spills, and the staff loves the way the product works and performs.

Q-FLO delivers all of the metrics we seek: Safety, easy-to-use, and superior in its performance with zero residual drug in the device.


~ Matt, Oncology Associates

WHAT CUSTOMERS LIKE ABOUT THE BREAKTHROUGH q-fLO™​ CONNECTOR

  • One device, not many
  • Fully USP 800 and USP 797 compliant
  • Easy to use
  • The audible and visual clues for when fluid path is open or closed
  • Universally compatible will all tubes and apparatuses used
  • Far more reliable than previously used connectors

Why is the Q-FLO™ connector so badly needed today?
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Repeated exposure to chemotherapy and other toxic drugs through spills or vapor can cause serious long-term damage to healthworker health.

​A spill can be as small as a tiny drop of drug--even microscopic--and still cause great damage.

But what's the actual risk? What is USP 800? And how does USP 800 protect your company?

The following 6-minute video answers these questions:
USP 800: What are the risks?

HEALTH RISKS OF EXPOSURE TO HAZARDOUS DRUGS

  • Headaches
  • Nausea and vomiting
  • Skin Rashes
  • Allergetic-type reactions
  • Hair loss
  • Organ damage
  • Infertility
  • Birth defects
  • Miscarriage
  • Cancer
  • More
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means of exposure

  • Inhalation
  • Skin absorption
  • Ingestion
  • Injection (needle stick)

USP 800/USP 797

On December 1, 2019, the US government health agencies mandated the use of Closed System Transfer Devices (CSTD) to protect healthworkers who work with hazardous drugs.

USP 800 is for bedside and administration, and USP 797 is for pharmacists.

What's your best course of action to protect your company and your employees?
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The only way to fully protect healthworkers and pharmacists from exposure to hazardous drugs is to ensure that the drug they're working with cannot enter their body in any way.

The new Q-FLO™ connector does just that in a way that makes it easy to work with.
What is Q-FLO™?
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THE HIGHEST QUALITY CSTD AVAILABLE

  • Closed, no drip, valved connectors
  • Fluid path closed prior to disconnection
  • Universal interoperability as it works with all female leurs and all attachments
  • Visual and auditory indicators confirm secure, sealed connection
  • Reduces the number of components required
  • Higher flow rate than other CSTDs available
  • Complete and safe swabbing ability; compatible with alcohol caps commonly used
  • Spin lock safely connects and disconnects, even with pressure in infusion line
  • Very low residual volume
  • Compliant with the National Institute of Occupational Safety and Health (NIOSH) protocol, superior test results compared to all other competitors
  • Compliant with all USP 800 and USP 797 requirements
  • ​Meets the requirements for the FDA 510(k) protocol​​​​

KEY END-USER ADVANTAGES

  • Exceptional, consistent safety
  • Peace of mind
  • Save time and effort with the fastest and easiest solution to apply
  • Enjoy ease-of-use with fewer components to manage
  • Enjoy job more

KEY BUSINESS OWNER ADVANTAGES

  • Ensure healthworker and patient safety
  • Enhance employee loyalty due to a greater employee experience
  • Reduce costs by eliminating failures and by reducing the number of components needed  
  • Enjoy outstanding superior performance and customer service

​How do the Q-FLO™ connectors work?

The following very short videos answer this question.
Compounding of Hazardous Drugs ​Using the Q-FLO™ Connector ​
Administration of Hazardous Drugs Using the Q-FLO™ Connector
A Closer Look
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The Q-FLO™ Connector PDF
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Instructions for Use PDF
What is the full range of solutions offered?
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The Q-FLO™ products incorporate quality components and tubing with the Q-FLO™ and/or the X-Needleless IV Connector bonded during manufacturing.

These products and sets eliminate the potential for accidental disconnects during the hazardous drug preparations and administrations.

Complete and ready-to-go, these  packaged products are cost-effective compared to self-assembly and reduce set-up time for both pharmacists and healthworkers.
Q-FLO™ Syringe Family
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Q-FLO™​ SYRINGES are available in 1ml, 3ml, 5ml, 10ml, 20ml, 30ml, and 50/60ml sizes for HD drug preparation as well as IV push administrations.
Q-FLO™ Secondary IV Sets
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​Q-FLO™ Secondary IV Sets are available with a bag spike, drip chamber with built-in X-Needleless IV Connector ADD-Port and Q-FLO™. Secondary IV Sets with these components and a 0.2 micron filter is also available.
Vial Access Devices
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Vial Access Devices are available for hazardous drug preparation. These are equipped with the X-Needleless IV Connector, CAP for 13mm, 20mm, 28mm top Vials, and a bladder designed to capture vapors displaced during hazardous drug reconstitution. ​Vial Access Devices are also available for diluent/non-hazardous Drugs.
A Closer Look
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The Q-FLO™ Family PDF
What if the Q-FLO™ CSTD could create a permanent connection?
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Q-LOC™ is a Closed System Transfer Device (CSTD) that consists of a Male Luer Connector that is a sterile, non-pyrogenic, and single-use device.

It enables healthcare professionals to handle fluids, including hazardous materials, such as chemotherapy, radioactive isotopes, and blood products when used in conjunction
with a compatible female luer connector. This includes the preparation and administration
of hazardous drugs.

Building off the unique Q-FLO™ design and technology, Q-LOC™ has the added benefit of once attached to a separate device and the cap is removed, the Q-LOC™  “spins” and cannot be detached. This provides a permanent connection.

This additional feature provides further safety to the healthcare worker while also allowing greater flexibility in devices that it can be attached to as it does not need to be bonded to a device. 

This saves significant time and money.
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Q-LOC™,  like Q-FLO™, is universal in the systems / female leur devices it can be bonded to.

What is Q-LOC™?
​A Closer Look
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The Q-LOC™ Flyer PDF
Who's behind the development of these game-changing solutions?
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  • A CEO with extensive experience as a founder, CEO, and COO of a variety of global businesses, including the NFL Europe, LLPG, and Cobra Golf Europe
  • A Founder and Chairman with 30+ years of experience in the medical device industry
  • Another Founder with over 20 years of experience in the medical device industry
  • Another Founder and CEO of a highly-successful manufacturing operation of medical device products
  • A total of 24 issued patents (US, EU, Japan, Canada, Australia
  • 2 additional patents allowed (Canada)
  • 2 additional patents pending (EU, Canada)
  • 510(k) marketing clearance from the US FDA
A Closer Look
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Who Infusion Innovations Is PDF
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Peter Smith, CEO
​949.205.9857
peter@infusioninnovations.net
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Infusion Innovations, Inc. (I3)
7514 Girard Ave, ste. 1231
La Jolla, CA  92037
949.205.9857
​peter@infusioninnovations.net
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