Profile: Medtronic, Inc. specializes in medical technology, thus providing lifelong solutions for people with chronic pain. We focus on cardiac rhythm disease management (CRDM), spinal & biologics, cardiovascular, neuromodulation, diabetes, and surgical technologies. Our cardiac resynchronization therapy (CRT) devices for heart failure include, Consulta™ CRT defibrillator, Maximo™ CRT defibrillator, Concerto™ CRT defibrillator, Insync Maximo™ CRT defibrillator and Carelink remote monitoring network. CRDM's primary product lines are implantable pacemakers, implantable cardioverter-defibrillators (ICDs), implantable cardiac resynchronization therapy devices and monitoring systems. Our latest ICDs include a feature called OptiVol fluid monitoring, which allows physicians to continually track their patient's fluid status using intrathoracic impedance (changes in the fluid flow). It provides trending data so that physicians can adjust medical treatment for patients at risk of acute decompensated heart failure. We also provide a unique, insertable diagnostic monitor for implantable pacemakers that can help physicians determine if unexplained fainting may be the result of an abnormally slow heart rhythm.

The company was founded in 1976, has revenues of USD 1-5 Million, has ~50 employees and is CE certified.

FDA Registration Number: 2182208

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• Left Ventricular Circulatory Assist Unit (FDA Code: DSQ)

• Liquid Bandage (FDA Code: KMF / 880.5090) A liquid bandage is a sterile device that is a liquid, semiliquid, or powder and liquid combination used to cover an opening in the skin or as a dressing for burns. The device is also used as a topical skin protectant.

• Liver Biopsy kit

• Lumboperitoneal Shunts

• Mechanical Heart Valve (FDA Code: LWQ)

• Membrane Lung for Long-Term Respiratory Support (FDA Code: BYS / 870.4100) A membrane lung for long-term pulmonary support is a device used to provide to a patient extracorporeal blood oxygenation for longer than 24 hours.

• Microdiscectomy Tools

• Miniature Pressure Transducer (FDA Code: IKE / 890.1615) A miniature pressure transducer is a device intended for medical purposes to measure the pressure between a device and soft tissue by converting mechanical inputs to analog electrical signals.

• Nasogastric Weighted Feeding Tubes

• Needle EMG Electrodes, Autoclaveable Concentric

• Needle EMG Electrodes, Disposable Concentric

• Needle EMG Electrodes, Disposable Hypodermic

• Needle EMG Electrodes, Disposable Monopolar

• NeoGuardr Temperature Probes

• Neurostimulator

• Non-Adhesive Bandages

• Non-invasive Magnetic Stimulation System

• Non-Invasive Tubing (FDA Code: GAZ / 880.6740) A vacuum-powered body fluid suction apparatus is a device used to aspirate, remove, or sample body fluids. The device is powered by an external source of vacuum. This generic type of device includes vacuum regulators, vacuum collection bottles, suction catheters and tips, connecting flexible aspirating tubes, rigid suction tips, specimen traps, noninvasive tubing, and suction regulators (with gauge).

• NuPrep, Ten20, Gel, Tapes

• Odontoid Fixation

• Open Urethral Catheterization Trays

• Open-End Urethral Catheter

• Open-ended Tapered Tip Urethral Catheter

• Orthopedic Knife (FDA Code: HTS / 888.4540) An orthopedic manual surgical instrument is a nonpowered hand-held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery. This generic type of device includes the cerclage applier, awl, bender, drill brace, broach, burr, corkscrew, countersink, pin crimper, wire cutter, prosthesis driver, extractor, file, fork, needle holder, impactor, bending or contouring instrument, compression instrument, passer, socket positioner, probe, femoral neck punch, socket pusher, reamer, rongeur, scissors, screwdriver, bone skid, staple driver, bone screw starter, surgical stripper, tamp, bone tap, trephine, wire twister, and wrench.

• Orthopedic Manual Surgical Instrument (FDA Code: LXH / 888.4540)

• Other Catheter

• P.V.C Infant Feeding Tubes

• Pacemaker Lead

• Paradigm Real-Time Pumps

• Pediatric Nasogastric Feeding Tubes

• Pediatric Open-End Urethral Catheters

• Pediatric Skin Temperature Probes

• Pediatric Urethral Catheters

• Pediatric Urine Collector (FDA Code: KNX / 876.5250) A urine collector and accessories is a device intended to collect urine. The device and accessories consist of tubing, a suitable receptacle, connectors, mechanical supports, and may include a means to prevent the backflow of urine or ascent of infection. The two kinds of urine collectors are:

• PEG Feeding Tubes/Kits

• Percutaneous Catheter (FDA Code: DQY / 870.1250) A percutaneous catheter is a device that is introduced into a vein or artery through the skin using a dilator and a sheath (introducer) or guide wire.

• Percutaneous Catheters Sets, Pediatric

• Percutaneous Catheters Sets, Pediatric Percutaneous Access

• Percutaneous Transluminal Coronary Angioplasty Catheter (FDA Code: LOX / 870.5100)

• Perfusion Apparatus (FDA Code: KJH / 864.2240) Cell and tissue culture supplies and equipment are devices that are used to examine, propagate, nourish, or grow cells and tissue cultures. These include such articles as slide culture chambers, perfusion and roller apparatus, cell culture suspension systems, and tissue culture flasks, disks, tubes, and roller bottles.

• Permanent Cardiac Pacemaker (FDA Code: DTB / 870.3680) A temporary pacemaker electrode is a device consisting of flexible insulated electrical conductors with one end connected to anexternal pacemaker pulse generator and the other end applied to the heart. The device is used to transmit a pacing electrical stimulus from the pulse generator to the heart and/or to transmit the electrical signal of the heart to the pulse generator.

• pH Monitor

• pH Monitoring System

• Plasma Coagulation Control (FDA Code: GGN / 864.5425) A multipurpose system for in vitro coagulation studies is a device consisting of one automated or semiautomated instrument and its associated reagents and controls. The system is used to perform a series of coagulation studies and coagulation factor assays.

• Pneumatic Tourniquet (FDA Code: KCY / 878.5910) A pneumatic tourniquet is an air-powered device consisting of a pressure-regulating unit, connecting tubing, and an inflatable cuff. The cuff is intended to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery.

• Polyurethane Feeding Tubes

• Pre-wired HeadCap

• Preconnected Urethral Catheterization Tray

• Pressure Regulators with Flow Control Valves

• Probes (FDA Code: HXB / 888.4540)