Profile: Baxter International Inc. provides medicines for hemophilia, immune disorders, kidney disease and cancer. We manufacture plasma-based and recombinant proteins used to treat hemophilia. We offer biopharmaceutical products which include plasma-based therapies to treat immune disorders, alpha 1 antitrypsin deficiency and other chronic blood-related conditions. We deliver biosurgery products for hemostasis, wound-sealing and tissue regeneration. We produce intravenous (IV) solutions & administration sets, premixed drugs & drug reconstitution systems, pre-filled vials and syringes for injectable drugs. Our product suprane (desflurane, USP), a nonflammable liquid administered through vaporizer, is a general inhalation anesthetic. It is indicated as an inhalation agent for induction and/or maintenance of anesthesia for inpatient and outpatient surgery in adults. Our prefilled syringes for PCA pumps are individually packaged for easy storage and administration. It is color-coded for easy identification. It is packaged 10 per case & has tamper-evident syringe caps.

The company was founded in 1931. NYSE:BAX (SEC Filings)

FDA Registration Number: 2025695

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• 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.

• Catheter Adaptor (FDA Code: GCE / 878.4200)

• Cervical Caps (FDA Code: HDR / 884.5250) A cervical cap is a flexible cuplike receptacle that fits over the cervix to collect menstrual flow or to aid artificial insemination. This generic type of device is not for contraceptive use.

• Chairs & stools

• Chronic Catheter Accessories

• Coagulation Factor Deficient Plasma (FDA Code: GJT / 864.7290) A factor deficiency test is a device used to diagnose specific coagulation defects, to monitor certain types of therapy, to detect coagulation inhibitors, and to detect a carrier state (a person carrying both a recessive gene for a coagulation factor deficiency such as hemophilia and the corresponding normal gene).

• Coats, Jackets & Smocks

• Collagen-Based Absorbable Hemostatic Agent (FDA Code: LMF / 878.4490) An absorbable hemostatic agent or dressing is a device intended to produce hemostasis by accelerating the clotting process of blood. It is absorbable.

• Compact Anesthesia Monitor

• Constant-flow Infusion Pump

• Coronary Guide Catheters

• Cotton Towels

• Cyclodialysis Spatulas

• Defibrillators

• Depolarising Muscle Relaxants

• Dialysis Catheters

• Dialysis Equipment

• Dialysis Solution

• Dialysis Solution With Dextrose

• Dialysis System

• Dialysis Units

• Direct Patient Interface Respiratory Gas Humidifier (FDA Code: BTT / 868.5450) A respiratory gas humidifier is a device that is intended to add moisture to, and sometimes to warm, the breathing gases for administration to a patient. Cascade, gas, heated, and prefilled humidifiers are included in this generic type of device.

• Disposable Leg Bags

• Disposable Needles

• Disposable Peritoneal Dialysis Administration Kit (FDA Code: KDJ / 876.5630) (1) A peritoneal dialysis system and accessories is a device that is used as an artificial kidney system for the treatment of patients with renal failure or toxemic conditions, and that consists of a peritoneal access device, an administration set for peritoneal dialysis, a source of dialysate, and, in some cases, a water purification mechanism. After the dialysate is instilled into the patient's peritoneal cavity, it is allowed to dwell there so that undesirable substances from the patient's blood pass through the lining membrane of the peritoneal cavity into this dialysate. These substances are then removed when the dialysate is drained from the patient. The peritoneal dialysis system may regulate and monitor the dialysate temperature, volume, and delivery rate together with the time course of each cycle of filling, dwell time, and draining of the peritoneal cavity or manual controls may be used. This generic device includes the semiautomatic and the automatic peritoneal delivery system.

• Disposable PVC Peritoneum Dialysis Bag

• Disposable Syringes

• Double Ended Cyclodialysis Spatula

• Dual Lumen Fistula Needle

• Dual-Channel Volumetric Infusion Pump

• Ear & Air Syringes

• Elastomeric Infusion Pump (FDA Code: MEB / 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.

• Electronystagmography

• Electronystagmography (ENG) Systems

• Endoscopes

• Endoscopes

• Endoscopes

• Endoscopes, Stabilization and Steering

• Endoscopy & Endoscopes

• Enema Supplies

• Enteral Irrigation Kit w/Piston Syringe

• Evacuated Bottle

• Evacuated Container

• Exam Table Paper

• Examination Drapes & Sheets

• Fistula Needle (FDA Code: FIE / 876.5540) A blood access device and accessories is a device intended to provide access to a patient's blood for hemodialysis or other chronic uses. When used in hemodialysis, it is part of an artificial kidney system for the treatment of patients with renal failure or toxemic conditions and provides access to a patient's blood for hemodialysis. The device includes implanted blood access devices, nonimplanted blood access devices, and accessories for both the implanted and nonimplanted blood access devices.

• Fluid Delivery Tubing (FDA Code: FPK / 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.

• Gas Cylinder Pressure Regulator (FDA Code: CAN / 868.2700) A pressure regulator is a device, often called a pressure-reducing valve, that is intended for medical purposes and that is used to convert a medical gas pressure from a high variable pressure to a lower, more constant working pressure. This device includes mechanical oxygen regulators.

• Gaseous Phase Enflurane Gas Analyzer (FDA Code: CBQ / 868.1500) An enflurane gas analyzer is a device intended to measure the concentration of enflurane anesthetic in a gas mixture.

• Gastro-Intestinals