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ContinueLearn More XTRICOR Systems is an FDA registered, ISO 13485:2016 certified design and medical manufacturing facility. Founded in 1976, TRICOR Systems has successfully provided high quality products and services to the medical market place.
SECTOR: Company Insight
TRICOR Systems is an FDA registered, ISO 13485:2016 certified design and medical manufacturing facility. Founded in 1976, TRICOR Systems has successfully provided high quality products and services to the medical market place.
TRICOR Systems is an FDA registered, ISO 13485:2016 certified design and medical manufacturing facility. Founded in 1976, TRICOR Systems has successfully provided high quality products and services to the medical market place.
We possess the expertise to design, develop, validate, and manufacture Class I, II and III electronic medical devices. Whether you are looking for a complete turnkey solution, or just supplementing your internal capabilities, TRICOR has the background and flexibility to meet your requirements. We offer the opportunity to confidently outsource your project needs.
After years of manufacturing the LifePort Kidney Transporter (LKT) medical devices, TRICOR Systems was integral to the design and development of the LifePort Liver Transporter (LLT). Similar to the LKT, the LLT utilizes a peristaltic pump to perfuse the liver during transport to provide a more viable organ for transplantation.
TRICOR designed the electrical portion and developed the software for the medical award winning STA. TRICOR is currently manufacturing the STA, which is a single tooth computer-controlled local anesthesia delivery system that ensures virtually pain-free, and ultimately fear-free injections. TRICOR assisted in writing the technical portion of the FDA 510K submittal for this Class II device.
The CompuFlo unit is a computer-controlled anesthesia delivery system for epidurals. TRICOR was commissioned to design a prototype and to support doctors with the development of a safer epidural spinal injection. TRICOR also assisted in writing the technical portion of the FDA 510K submittal for this Class II device in which the submittal was approved the first time through.
TRICOR Systems Inc. was approached with an idea of developing a device to dry the internal channels of endoscopes after they had been cleaned and disinfected. The idea was conceived after several deaths were blamed on improperly cleaned endoscopes. Within months, TRICOR had completed the proof of concept, prototypes and production units. These Class I Exempt devices push HEPA-filtered air though tubing and disposable fittings into the internal channels of an endoscope.
The Wand™ is a computer-controlled local anesthesia delivery system that ensures virtually pain-free and, ultimately, fear-free injections. Within a four month time frame TRICOR was delivering 1000 units per week. In the following years TRICOR was then chosen to perform the engineering, hardware redesign and manufacturing for the Wand Plus, Compu-Med and Compu-Dent.
TRICOR was commissioned to take over manufacturing and later reengineered the TMX 2000 to the TMX 3000. The TMX3000 was a Class III device for treating the prostate. The TMX 3000 went end of life when it was replaced by a different technology.
TRICOR Systems electronic contract manufacturing capability is structured to produce a wide variety of products for its customers. TRICOR can manufacture small quantities of prototypes and pre-production units to large quantities such as the 50,000+ unit/year rate achieved on the Wand™ Dental System. Our experience with both Class I, II and III medical devices minimizes problems and facilitates quicker product turns. Changes or product updates are also streamlined due to TRICOR’s in-house engineering staff.
Our team of Engineers provide outstanding capability not found in many small companies. From the design of simple fixtures to complete systems, the attention given to performance, reliability and quality does not vary.
Each engineer is proficient in both hardware and software design. This capability increases efficiency and reduces cost as the engineer who writes the operating software is extremely knowledgeable with the hardware he/she is trying to control.
Electrical Engineering tools/aids: The latest state-of-the-art schematic capture and PCB layout tools from Mentor Graphics are used on all electrical design activities.
Mechanical Engineering tools/aids: To develop the highest quality mechanical items, we utilize both AutoCAD and the advanced 3-D solid modeling tools offered by Solidworks®.
As products become more sophisticated, medical device performance is highly dependent on reliable, verifiable and maintainable software. TRICOR has a history of providing embedded and PC-based architectures for numerous product requirements. By utilizing current development tools, coupled with a controlled design structure, the customer is ensured product and regulatory specifications are satisfied.
In addition to having the latest design tools, we have the staff and expertise to design and develop electronic systems that meet all domestic and international safety requirements (IEC 60601 or UL 2601 and CAN/CSA-C22.2 60601).
The Ultimate Drying Experience. Discover the Dri-Scope Aid Drying Difference
ANSI/AAMI ST91:2021 states that-The endoscope and its components should be dried after completion of the cleaning and disinfection process. Flexible endoscopes with channels should be dried for a minimum of 10-minutes with pressure-regulated forced instrument air or a minimum of HEPA-filtered air (Ofstead, 2018; Barakat, 2018; Perumpail, 2019; Alfa, 1991).
The Dri-Scope Aid® Jet~Stream is available in two models. The model 1840P acts as a standalone unit where the internal pump provides HEPA-filtered air with constant flow and consistent pressure with repeatable results. The model 1840R is ideal for users that wish to use medical or instrument air.
The Jet Drying stations provide an additional work area to dry the internal channels of your endoscopes safely. The Dri-Scope Aid® Jet-Stream is attached to the integrated pole on either the Jet-Cart or Jet-Pole. The Dri-Scope® Aid Jet-Stream provides HEPA-filtered or Instrument air to all the internal channels of an endoscope after reprocessing. The Jet-Stream (sold separately) can dry up to two scopes simultaneously.
SteriView is the next generation of advanced small diameter, near field inspection scopes designed to provide ready access to and imaging of the interior chambers, lumens and working channels of endoscopes and surgical instruments.
Dri-Scope Aid® Family of Products Assists in the Drying of the Internal Channels of an Endoscope.