Trivirix

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Web: http://www.trivirix.com
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Address: 925, 6th Avenue NE, Milaca, Minnesota 56353, USA
Phone: +1-(320)-982-8000 | Fax: +1-(320)-982-8001 | Map/Directions >>

Profile: Trivirix is a full service contract manufacturing company that is focused on the manufacture and design support of complex electro-mechanical medical, diagnostic, analytical and life-science devices. We are ISO 9001 & ISO 13485 certified, FDA registered and QSR compliant. Our contract manufacturing product list comprises of DuPont Riboprinter, neoprobe® GDS, volumetric infusion pump, and vital sign/conscious sedation monitor. Neoprobe® GDS is a gamma detection control unit widely used in surgical procedures such as sentinel lymph node biopsy (SLN). The SLN provides a minimally invasive technique for evaluating the potential spread of cancer to lymph nodes and other organs.

The company was founded in 1998, has revenues of USD 10-25 Million, has ~90 employees and is CE certified.

FDA Registration Number: 2183613

17 Products/Services (Click for related suppliers)

• Blood and Plasma Warming Device (FDA Code: KZL / 864.9205)

A nonelectromagnetic blood and plasma warming device is a device that warms blood or plasma, by means other than electromagnetic radiation, prior to administration.

• Contract Manufacturers

• Dual Chamber Implantable Pulse-Generator (FDA Code: LWP)

• Electrocardiograph Transmitter/Receiver System (FDA Code: DXH / 870.2920)

A telephone electrocardiograph transmitter and receiver is a device used to condition an electrocardiograph signal so that it can be transmitted via a telephone line to another location. This device also includes a receiver that reconditions the received signal into its original format so that it can be displayed. The device includes devices used to transmit and receive pacemaker signals.

• External Pacemaker Pulse Generator (FDA Code: DTE / 870.3600)

An external pacemaker pulse generator is a device that has a power supply and electronic circuits that produce a periodic electrical pulse to stimulate the heart. This device, which is used outside the body, is used as a temporary substitute for the heart's intrinsic pacing sytem until a permanent pacemaker can be implanted, or to control irregular heartbeats in patients following cardiac surgery or a myocardial infarction. The device may have adjustments for impulse strength, duration, R-wave sensitivity, and other pacing variables.

• Implantable Electrical Stimulator (FDA Code: EZW / 876.5270)

An implanted electrical urinary device is a device intended for treatment of urinary incontinence that consists of a receiver implanted in the abdomen with electrodes for pulsed-stimulation that are implanted either in the bladder wall or in the pelvic floor, and a battery-powered transmitter outside the body.

• Implantable Spinal Cord Stimulator (FDA Code: GZB / 882.5880)

An implanted spinal cord stimulator for pain relief is a device that is used to stimulate electrically a patient's spinal cord to relieve severe intractable pain. The stimulator consists of an implanted receiver with electrodes that are placed on the patient's spinal cord and an external transmitter for transmitting the stimulating pulses across the patient's skin to the implanted receiver.

• Implanted Electrical Stimulator (FDA Code: MHY)

• Implanted Electrical Stimulator For Parkinsonian Symptoms (FDA Code: NHL)

• Implanted Peripheral Nerve Stimulator (FDA Code: GZF / 882.5870)

An implanted peripheral nerve stimulator for pain relief is a device that is used to stimulate electrically a peripheral nerve in a patient to relieve severe intractable pain. The stimulator consists of an inplanted receiver with electrodes that are placed around a peripheral nerve and an external transmitter for transmitting the stimulating pulses across the patient's skin to the implanted receiver.

• Implanted Programmable Infusion Pump (FDA Code: LKK)

• Implanted Sacral Nerve Stimulator

• Nuclear Uptake Probe (FDA Code: IZD / 892.1320)

A nuclear uptake probe is a device intended to measure the amount of radionuclide taken up by a particular organ or body region. This generic type of device may include a single or multiple detector probe, signal analysis and display equipment, patient and equipment supports, component parts, and accessories.

• Pacemaker Programmer (FDA Code: KRG / 870.3700)

A pacemaker programmer is a device used to change noninvasively one or more of the electrical operating characteristics of a pacemaker.

• Pacemaker Test Magnet (FDA Code: DTG / 870.3690)

A pacemaker test magnet is a device used to test an inhibited or triggered type of pacemaker pulse generator and cause an inhibited or triggered generator to revert to asynchronous operation.

• Radiofrequency Lesion Probe (FDA Code: GXI / 882.4725)

A radiofrequency lesion probe is a device connected to a radiofrequency (RF) lesion generator to deliver the RF energy to the site within the nervous system where a lesion is desired.

• Totally Implanted Spinal Cord Stimulator for Pain Relief (FDA Code: LGW)