Plexus Corp

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Contact: Mr. Phil Salditt - Marketing & Sales Communications
Web: http://www.plexus.com
E-Mail:
Address: 55 Jewelers Park Drive, P.O. Box 156, Neenah, Wisconsin 54957-0677, USA
Phone: +1-(920)-722-3451 | Fax: +1-(920)-751-5395 | Map/Directions >>

Profile: Plexus Corp is engaged in the electronic manufacturing services. Our solutions include mechanical, electronic and software design, printed circuit board development, prototyping services, new product introduction, material procurement & supply chain management, printed circuit board & higher level assembly, test development, in-circuit & functional testing, final system box build, fulfillment, service, and repair. We specialize in providing integrated product development, manufacturing, and sustaining services of medical products. Our product line includes imaging, monitoring, diagnostic and therapeutic products.

The company was founded in 1980, has revenues of > USD 1 Billion, has ~250 employees and is ISO 9001, CE certified. NASDAQ:PLXS (SEC Filings)

15 Products/Services (Click for related suppliers)

• AC-Powered Portable Ward Use Suction Apparatus (FDA Code: JCX / 878.4780)

A powered suction pump is a portable, AC-powered or compressed air-powered device intended to be used to remove infectious materials from wounds or fluids from a patient's airway or respiratory support system. The device may be used during surgery in the operating room or at the patient's bedside. The device may include a microbial filter.

• Arrhythmia Detector and Alarm (FDA Code: DSI / 870.1025)

The arrhythmia detector and alarm device monitors an electrocardiogram and is designed to produce a visible or audible signal or alarm when atrial or ventricular arrhythmia, such as premature contraction or ventricular fibrillation, occurs.

• Automatic Implantable Cardioverter-defibrillator (FDA Code: LWS)

• Contract Manufacturing

• Diagnostic Intravascular Catheter (FDA Code: DQO / 870.1200)

An intravascular diagnostic catheter is a device used to record intracardiac pressures, to sample blood, and to introduce substances into the heart and vessels. Included in this generic device are right-heart catheters, left-heart catheters, and angiographic catheters, among others.

• Diagnostic Ultrasonic Transducer (FDA Code: ITX / 892.1570)

A diagnostic ultrasonic transducer is a device made of a piezoelectric material that converts electrical signals into acoustic signals and acoustic signals into electrical signals and intended for use in diagnostic ultrasonic medical devices. Accessories of this generic type of device may include transmission media for acoustically coupling the transducer to the body surface, such as acoustic gel, paste, or a flexible fluid container.

• Durable Product Contract Manufacturing

• Engineering/Design Service

• Implantable Permanent Pulse Generator (FDA Code: NVZ)

• Infusion Pump Accessories (FDA Code: MRZ / 880.5725)

An infusion pump is a device used in a health care facility to pump fluids into a patient in a controlled manner. The device may use a piston pump, a roller pump, or a peristaltic pump and may be powered electrically or mechanically. The device may also operate using a constant force to propel the fluid through a narrow tube which determines the flow rate. The device may include means to detect a fault condition, such as air in, or blockage of, the infusion line and to activate an alarm.

• Liquid Crystal Vein Location Device (FDA Code: KZA / 880.6970)

A liquid crystal vein locator is a device used to indicate the location of a vein by revealing variations in the surface temperature of the skin by displaying the color changes of heat sensitive liquid crystals (cholesteric esters).

• 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.

• Programmable Implantable Heart Pacemaker (FDA Code: DXY / 870.3610)

An implantable 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 is used as a substitute for the heart's intrinsic pacing system to correct both intermittent and continuous cardiac rhythm disorders. This device includes triggered, inhibited, and asynchronous devices implanted in the human body.

• Ultrasonic Puls-Echo Scanner (FDA Code: IYO / 892.1560)

An ultrasonic pulsed echo imaging system is a device intended to project a pulsed sound beam into body tissue to determine the depth or location of the tissue interfaces and to measure the duration of an acoustic pulse from the transmitter to the tissue interface and back to the receiver. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.

• Ultrasonic Pulsed Doppler Imaging System (FDA Code: IYN / 892.1550)

An ultrasonic pulsed doppler imaging system is a device that combines the features of continuous wave doppler-effect technology with pulsed-echo effect technology and is intended to determine stationary body tissue characteristics, such as depth or location of tissue interfaces or dynamic tissue characteristics such as velocity of blood or tissue motion. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.