IDM, a Haemonetics Company

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Contact: Timothy Coburn - President
Web: http://www.idm.com
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Address: 9701 W. Higgins Road, Suite 500, Rosemont, Illinois 60018, USA
Phone: +1-(847)-825-2300, 800-249-4276 | Fax: +1-(847)-825-2303 | Map/Directions >>

Profile: IDM, a Haemonetics Company is a developer of software for blood centers, plasma centers, and medical device manufacturers. We specialize in blood collection technology. We provide software applications for blood collection, blood laboratory operations, and services. Our product lines aid customers in donor management and recruitment, blood component management, & federal guideline compliance. Our Surround provides a secure, adaptable and reliable solution to handle the time-critical and regulated laboratory needs. It is an open and flexible laboratory system that can be interfaced with current & future testing instruments & host systems. It allows blood banks to customize a default test panel while tracking sample results either automatically or manually.

The company was founded in 1977, has revenues of USD 5-10 Million, has ~60 employees. NYSE:HAE (SEC Filings)

29 Products/Services (Click for related suppliers)

• Activated Whole Blood Clotting Time (FDA Code: JBP / 864.7140)

An activated whole blood clotting time tests is a device, used to monitor heparin therapy for the treatment of venous thrombosis or pulmonary embolism by measuring the coagulation time of whole blood.

• Automated Coagulation Analyzer (FDA Code: GKP / 864.5400)

A coagulation instrument is an automated or semiautomated device used to determine the onset of clot formation for in vitro coagulation studies.

• Automated Coagulation Instrument (FDA Code: GKP / 864.5400)

• Automated Platelet Aggregation System (FDA Code: JOZ / 864.5700)

An automated platelet aggregation system is a device used to determine changes in platelet shape and platelet aggregation following the addition of an aggregating reagent to a platelet-rich plasma.

• 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 & Components Collection Container (FDA Code: KSR / 864.9100)

An empty container for the collection and processing of blood and blood components is a device intended for medical purposes that is an empty plastic bag or plastic or glass bottle used to collect, store, or transfer blood and blood components for further processing.

• Blood Bank Software (FDA Code: MMH / 864.9175)

An automated blood grouping and antibody test system is a device used to group erythrocytes (red blood cells) and to detect antibodies to blood group antigens.

• Blood Banking Products

• Blood Clot Coagulation Analyzer (FDA Code: GKP / 864.5400)

• Blood Donor Chair (FDA Code: FML / 880.6140)

A medical chair or table is a device intended for medical purposes that consists of a chair or table without wheels and not electrically powered which, by reason of special shape or attachments, such as food trays or headrests, or special features such as a built-in raising and lowering mechanism or removable arms, is intended for use of blood donors, geriatric patients, or patients undergoing treatment or examination.

• Blood Mixing and Weighing Device (FDA Code: KSQ / 864.9195)

A blood mixing device is a device intended for medical purposes that is used to mix blood or blood components by agitation. A blood weighing device is a device intended for medical purposes that is used to weigh blood or blood components as they are collected.

• Blood Storage Freezer (FDA Code: KSE / 864.9700)

A blood storage refrigerator and a blood storage freezer are devices intended for medical purposes that are used to preserve blood and blood products by storing them at cold or freezing temperatures.

• Blood Transfer Unit (FDA Code: KSB / 864.9875)

A transfer set is a device intended for medical purposes that consists of a piece of tubing with suitable adaptors used to transfer blood or plasma from one container to another.

• 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.

• Catheter Accessories (FDA Code: KGZ / 878.4200)

An introduction/drainage catheter is a device that is a flexible single or multilumen tube intended to be used to introduce nondrug fluids into body cavities other than blood vessels, drain fluids from body cavities, or evaluate certain physiologic conditions. Examples include irrigation and drainage catheters, pediatric catheters, peritoneal catheters (including dialysis), and other general surgical catheters. An introduction/drainage catheter accessory is intended to aid in the manipulation of or insertion of the device into the body. Examples of accessories include adaptors, connectors, and catheter needles.

• Coagulation Analyzer with Timer (FDA Code: GKP / 864.5400)

• Coagulation Analyzers (FDA Code: GKP / 864.5400)

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

• Disposable Hot/Cold Pack (FDA Code: IMD / 890.5710)

A hot or cold disposable pack is a device intended for medical purposes that consists of a sealed plastic bag incorporating chemicals that, upon activation, provides hot or cold therapy for body surfaces.

• Frozen Blood Processor (FDA Code: KSW / 864.9145)

A processing system for frozen blood is a device used to glycerolize red blood cells prior to freezing to minimize hemolysis (disruption of the red cell membrane accompanied by the release of hemoglobin) due to freezing and thawing of red blood cells and to deglycerolize and wash thawed cells for subsequent reinfusion.

• Heat-Sealing Device (FDA Code: KSD / 864.9750)

A heat-sealing device is a device intended for medical purposes that uses heat to seal plastic bags containing blood or blood components.

• Manual/Powered Portable Aspiration Pump (FDA Code: BTA / 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.

• Multipurpose System for Invitro Coagulation Studies (FDA Code: JPA / 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.

• Non-Pneumatic Tourniquet (FDA Code: GAX / 878.5900)

A nonpneumatic tourniquet is a device consisting of a strap or tubing intended to be wrapped around a patient's limb and tightened to reduce circulation.

• 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.

• Shaker/Stirrer (FDA Code: JRQ / 862.2050)

• Short-Term Less Than 30 Days Therapeutic Intravascular Catheter (FDA Code: FOZ / 880.5200)

An intravascular catheter is a device that consists of a slender tube and any necessary connecting fittings and that is inserted into the patient's vascular system for short term use (less than 30 days) to sample blood, monitor blood pressure, or administer fluids intravenously. The device may be constructed of metal, rubber, plastic, or a combination of these materials.

• Therapeutic Automated Blood Cell and Plasma Separator (FDA Code: LKN)

• Whole Blood Plasma (FDA Code: DGQ / 866.5700)

A whole human plasma or serum immunological test system is a device that consists of reagents used to measure by immunochemical techniques the proteins in plasma or serum. Measurements of proteins in plasma or serum aid in the diagnosis of any disease concerned with abnormal levels of plasma or serum proteins, e.g., agammaglobulinemia, allergies, multiple myeloma, rheumatoid vasculitis, or hereditary angioneurotic edema.