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Our Mission Statement
- to You, the Customer:
"It is Medcomp®'s goal to provide only the highest quality product and service to assure total customer satisfaction and to meet customer requirements."
Medcomp® Corporate Headquarters in Harleysville, PA

Our History
Medcomp® was founded in 1978 to produce and market Vascular Access Catheters for acute hemodialysis. At that time, catheter technology was in its early stages of development. The designs were simple, consisting of a single lumen catheter for single needle dialysis or double lumen catheters for continuous flow dialysis. Since the early 80’s, our engineering and applications expertise have been put to work to provide a superior catheter to meet the increasing demand for a better product for a changing market.
Research and development by our in-house staff of engineers, working in conjunction with some of today’s preeminent physicians in the field of vascular access, has allowed us to provide our customers with some of the most innovative vascular access technology available today. From our Canaud and Tesio® Catheters (Dr. Bernard Canaud, France and Dr. Franco Tesio, Italy) to our Raulerson Duo-Flow™ (Dr. J. Daniel Raulerson, USA) and our recent Split Cath® (Dr. Stephen Ash, USA), we are continually improving on existing technology by providing a biocompatible, durable, high flow catheter to suit every need. The medical community is encouraged to submit suggestions, opinions, or comments regarding product function, design or development. This philosophy has been the cornerstone of Medcomp®’s growth.
Marketing and distribution of our vascular access products is accomplished through 11 United States distributors and over 85 International distributors. Medcomp® is a global market leader, tailoring our products and technology to the demands of several geographic markets. Current marketing networks and a wealth of intellectual property assure Medcomp®’s leadership in the years to come.

Quality
Medcomp® Quality comes first. Our Quality System is ISO 13485 certified by KEMA Registered Quality. As a medical device manufacturer, we also maintain certification to Annex II, a full quality system as defined in the Medical Device Directive 93/42 EEC, certified by NV KEMA, Arnhem, the Netherlands. A staff of qualified Auditors accomplish internal and external (subcontractor) auditing on a regularly scheduled basis.
We also provide registration support to all international distributors by assisting with formalization and legalization of documents as required by their governments.

Engineering
Our Engineering Department is staffed with a diversely disciplined group of product development engineers, specializing in biomedical, mechanical and electrical engineering, with over 50 years of combined experience in medical device design, research, and development.
In the last five years, Medcomp® engineers have been dedicated to developing unique vascular access products that combine cutting-edge manufacturing processes and technology with advanced designs to produce products that are enthusiastically accepted while dominating the vascular access market.
All Medcomp® products are developed in accordance with all FDA Quality Systems Regulations, European Medical Device Directives (CE), Japanese GMPi and numerous other international regulations and standards. Adherence to these regulations and standards ensures that product development is completed with safety and performance as the primary goal. Working directly with physicians and other medical professionals assures that new products consistently meet the clinical needs of the medical community.

Production
Our in-house Production Department is busy around the clock to provide our customers with finished, packaged devices. The clean working environment provides our customers with a wide range of device and accessory packaging. From finished device manufacturing, to wrapping, sealing and inspecting, our Production Department is fully equipped to handle all aspects of device finishing and packaging. Stringent controls and procedures assure a quality product, whether you are ordering a standard catalog item, or customized product for your specific needs.

Our Future Together
As we enter the 21st century, we will continue to be on the forefront of the medical device community by providing the most innovative and advanced access technology available. As the demand for improved vascular access grows, so will Medcomp®.

  PNW133 Rev. C 10/04