About Procedure Products
Procedure Products, Inc., founded in 1985, is a United States based firm which is registered and inspected by the Federal Food and Drug Administration and holds certification to the ISO 13485 standard. The company has 510(k) authorization from the Federal Food and Drug Administration to manufacture numerous hospital special-procedure needles as well as our signature non-glare color-coded syringes and special control syringes in a wide variety of sizes and colors. We also manufacture the following items specifically designed for Radiology and Cardiology: Guide-wire Torque Devices, Waste Fluid Systems, Adapters and High Pressure Connectors.
Procedure Products supplies products of extremely high quality at a very competitive price. Procedure Products has the agility and flexibility to rapidly respond to the changing needs of our customers. We are the supplier of choice for custom kit and pack manufacturers because of our award-winning service and our innovative products.
Important: Joint Commision, 2009 National Patient, Safety Goals Elements of Performance for NPSG.03.04.01
Labeling occurs when any medication or solution is transferred from the original packaging to another container.
Meet the Team
Richard Bynum, CEO
Richard began his medical device career in the implantable heart pacemaker industry, working in various sales and management positions for Cordis, Eli Lilly, Siemens, and St. Jude Medical.
Richard acquired Procedure Products in 2007 with the goal of developing Procedure Products into the leading supplier of color-coded syringes for the medical industry. The bright future for Procedure Products energizes Richard as he works to build Procedure Products into the industry leader.
Mike Huiatt, CFO
Mike Huiatt, along with Richard Bynum, purchased Procedure Products on Oct. 1, 2007 after working in the Petroleum industry for many years. A CPA by trade since 1967, Mike serves as CFO where he oversees banking, money management, Federal and State tax & government reporting, Insurance, personnel and benefits, as well as financial reporting for the company.
Clarice Arruda Gehrke, Plant Manager
Clarice Arruda is the General Manager of Procedure Products Inc. She started working at Procedure Products in 1988 at an entry level position. While enjoying her position, she often made note that some components could be of better quality. As you may be able to see, she is not afraid to speak her mind. She was recruited into the quality department shortly after she was hired, then soon into management. She still works closely with the quality department, as it is her passion to see that quality products are manufactured for the end users and their families. She currently resides in Vancouver, Washington.
Doug Rowley, Quality Manager
After studying Biology and Chemistry at Oregon State University, Doug spent a decade in the Medical Device and Pharmaceutical industry before joining the Procedure Products team in 2014. Doug has experience working in nearly all facets of the Medical Device industry, having begun his career in manufacturing and laboratory testing before transitioning into regulatory and quality assurance management roles. Doug has substantial experience working with domestic and international regulatory bodies for the purposes of obtaining new product approvals, and as the Management Representative during compliance audits. Doug has enjoyed working for Procedure Products due to the great people, fast-paced style of business, and the family-like atmosphere.