Dideco S.P.A.

Contact: S. Foshieri - National Sales Manager
Web: http://www.sorin-cp.com
Address: Via Statale #86 12 Nord, 86, Po Box 87, Mirandola, MO 41037, Italy
Phone: +39-(0535)-29811 | Fax: +39-(0535)-25229 | Map/Directions >>

Profile: Dideco S.P.A. focuses on perfusion and blood management systems. Our products include endoscopic vessel harvesting, cardiopulmonary equipment, oxygenators, optimized bypass systems, venous and cardiotomy reservoirs, arterial filters, cardioplegia, hemoconcentration, monitoring, centrifugal blood pump, cannulae and suckers, perfusion tubing sytems, autotransfusion and whole blood separation. Our ClearGlider uses an open CO2 system with no reliance on closed insufflations, and it carries a lower risk of CO2 embolism. It helps patients by reducing post-operative pain, scarring, and the length of stay in the hospital. Our synergy optimized bypass system's features include, fully integrated safest minibypass system with arterial filter, centrifugal pump, HE, and venous bubble trap integrated, fully phosphorylcholine coated. We offer hemoconcentrators, which do not need to be rinsed before use, thus enabling integration in the ECC after priming at any time during perfusion. It uses polyethersulfone fibre, and can be used for different patient sizes. Our Aortic cannulae are available with bent tip, and straight tip, and they have optimized tubing diameter for each size, gradually increasing from the tip to the connector.

The company has ~700 employees.

FDA Registration Number: 9680841
US Agent: Scott Light / Livanova Usa, Inc.
Phone: +1-(303)-467-6313 Fax: +1-(303)-467-6502 E-Mail:

20 Products/Services (Click for related suppliers)

• Arterial Line Cardiopulmonary Bypass Blood Filter (FDA Code: DTM / 870.4260)

A cardiopulmonary bypass arterial line blood filter is a device used as part of a gas exchange (oxygenator) system to filter nonbiologic particles and emboli (blood clots or pieces of foreign material flowing in the bloodstream which will obstruct circulation by blocking a vessel) out of the blood. It is used in the arterial return line.

• Autotransfusion Apparatus (FDA Code: CAC / 868.5830)

An autotransfusion apparatus is a device used to collect and reinfuse the blood lost by a patient due to surgery or trauma.

• Blood Transfusion Microfilter (FDA Code: CAK / 880.5440)

An intravascular administration set is a device used to administer fluids from a container to a patient's vascular system through a needle or catheter inserted into a vein. The device may include the needle or catheter, tubing, a flow regulator, a drip chamber, an infusion line filter, an I.V. set stopcock, fluid delivery tubing, connectors between parts of the set, a side tube with a cap to serve as an injection site, and a hollow spike to penetrate and connect the tubing to an I.V. bag or other infusion fluid container.

• Cardiopulmonary Bypass Accessories (FDA Code: KRI / 870.4200)

Cardiopulmonary bypass accessory equipment is a device that has no contact with blood and that is used in the cardiopulmonary bypass circuit to support, adjoin, or connect components, or to aid in the setup of the extracorporeal line, e.g., an oxygenator mounting bracket or system-priming equipment.

• Cardiopulmonary Bypass Adaptor (FDA Code: DTL / 870.4290)

A cardiopulmonary bypass adaptor, stopcock, manifold, or fitting is a device used in cardiovascular diagnostic, surgical, and therapeutic applications to interconnect tubing, catheters, or other devices.

• Cardiopulmonary Bypass Blood Reservoir (FDA Code: DTN / 870.4400)

A cardiopulmonary bypass blood reservoir is a device used in conjunction with short-term extracorporeal circulation devices to hold a reserve supply of blood in the bypass circulation.

• Cardiopulmonary Bypass Cardiotomy Return Sucker (FDA Code: DTS / 870.4420)

A cardiopulmonary bypass cardiotomy return sucker is a device that consists of tubing, a connector, and a probe or tip that is used to remove blood from the chest or heart during cardiopulmonary bypass surgery.

• Cardiopulmonary Bypass Cardiotomy Suction Line Blood Filter (FDA Code: JOD / 870.4270)

A cardiopulmonary bypass cardiotomy suction line blood filter is a device used as part of a gas exchange (oxygenator) system to filter nonbiologic particles and emboli (a blood clot or a piece of foreign material flowing in the bloodstream which will obstruct circulation by blocking a vessel) out of the blood. This device is intended for use in the cardiotomy suction line.

• Cardiopulmonary Bypass Defoamer (FDA Code: DTP / 870.4230)

A cardiopulmonary bypass defoamer is a device used in conjunction with an oxygenator during cardiopulmonary bypass surgery to remove gas bubbles from the blood.

• Cardiopulmonary Bypass Heart-Lung Machine Console (FDA Code: DTQ / 870.4220)

A cardiopulmonary bypass heart-lung machine console is a device that consists of a control panel and the electrical power and control circuitry for a heart-lung machine. The console is designed to interface with the basic units used in a gas exchange system, including the pumps, oxygenator, and heat exchanger.

• Cardiopulmonary Bypass Heat Exchanger (FDA Code: DTR / 870.4240)

A cardiopulmonary bypass heat exchanger is a device, consisting of a heat exchange system used in extracorporeal circulation to warm or cool the blood or perfusion fluid flowing through the device.

• Cardiopulmonary Bypass On-Line Blood Gas Monitor (FDA Code: DRY / 870.4330)

A cardiopulmonary bypass on-line blood gas monitor is a device used in conjunction with a blood gas sensor to measure the level of gases in the blood.

• Cardiopulmonary Bypass Oxygenator (FDA Code: DTZ / 870.4350)

A cardiopulmonary bypass oxygenator is a device used to exchange gases between blood and a gaseous environment to satisfy the gas exchange needs of a patient during open-heart surgery.

• Cardiopulmonary Bypass Vascular Catheter (FDA Code: DWF / 870.4210)

A cardiopulmonary bypass vascular catheter, cannula, or tubing is a device used in cardiopulmonary surgery to cannulate the vessels, perfuse the coronary arteries, and to interconnect the catheters and cannulas with an oxygenator. The device includes accessory bypass equipment.

• Cardiovascular Intravascular Filter (FDA Code: DTK / 870.3375)

A cardiovascular intravascular filter is an implant that is placed in the inferior vena cava for the purpose of preventing pulmonary thromboemboli (blood clots generated in the lower limbs and broken loose into the blood stream) from flowing into the right side of the heart and the pulmonary circulation.

• Catheter Cannula (FDA Code: DQR / 870.1300)

A catheter cannula is a hollow tube which is inserted into a vessel or cavity; this device provides a rigid or semirigid structure which can be connected to a tube or connector.

• Diagnostic Automated Blood Cell Separator (FDA Code: GKT / 864.9245)

• High Permeability with/without Sealed Dialysate System (FDA Code: KDI / 876.5860)

A high permeability hemodialysis system is a device intended for use as an artificial kidney system for the treatment of patients with renal failure, fluid overload, or toxemic conditions by performing such therapies as hemodialysis, hemofiltration, hemoconcentration, and hemodiafiltration. Using a hemodialyzer with a semipermeable membrane that is more permeable to water than the semipermeable membrane of the conventional hemodialysis system (876.5820), the high permeability hemodialysis system removes toxins or excess fluid from the patient's blood using the principles of convection (via a high ultrafiltration rate) and/or diffusion (via a concentration gradient in dialysate). During treatment, blood is circulated from the patient through the hemodialyzer's blood compartment, while the dialysate solution flows countercurrent through the dialysate compartment. In this process, toxins and/or fluid are transferred across the membrane from the blood to the dialysate compartment. The hemodialysis delivery machine controls and monitors the parameters related to this processing, including the rate at which blood and dialysate are pumped through the system, and the rate at which fluid is removed from the patient. The high permeability hemodialysis system consists of the following devices:

• Non-Roller Type Cardiopulmonary Bypass Blood Pump (FDA Code: KFM / 870.4360)

A nonroller-type cardiopulmonary bypass blood pump is a device that uses a method other than revolving rollers to pump the blood through the cardiopulmonary bypass circuit during bypass surgery.

• Refrigerated Centrifuges (FDA Code: JQC / 862.2050)

General purpose laboratory equipment labeled or promoted for a specific medical use is a device that is intended to prepare or examine specimens from the human body and that is labeled or promoted for a specific medical use.