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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• A.V. Fistula Needle

• A.V.Fistula Needle Set

• Absorbable Adhesion Barrier (FDA Code: MCN)

• Adult-Pediatric Volumetric Infusion Pumps

• Ambulatory Infusion Pumps

• Ambulatory Pumps

• Analgesics

• Anesthesia

• Anesthesia Delivery Unit

• Anesthesia Equipment

• Anesthesia Equipment

• Anesthesia Infusion Pump Tubing

• Anesthesia Monitor

• Anesthesia Ring

• Anesthesia Workstation

• Anesthetic Infusion Pump (FDA Code: FRN / 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.

• Anesthetics

• Anti-Regurgitation Valve with Blood Tubing Set (FDA Code: FJK / 876.5820) A hemodialysis 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 an extracorporeal blood system, a conventional dialyzer, a dialysate delivery system, and accessories. Blood from a patient flows through the tubing of the extracorporeal blood system and accessories to the blood compartment of the dialyzer, then returns through further tubing of the extracorporeal blood system to the patient. The dialyzer has two compartments that are separated by a semipermeable membrane. While the blood is in the blood compartment, undesirable substances in the blood pass through the semipermeable membrane into the dialysate in the dialysate compartment. The dialysate delivery system controls and monitors the dialysate circulating through the dialysate compartment of the dialyzer.

• Antihistamines

• Antihistamines and Decongestants

• Arterial Venous Fistula Needle

• Arthroscopes (FDA Code: HRX / 888.1100) An arthroscope is an electrically powered endoscope intended to make visible the interior of a joint. The arthroscope and accessories also is intended to perform surgery within a joint.

• Aspiration Syringe

• Aspirators

• Automatic Defibrillators

• Automatic Delivery Peritoneal System (FDA Code: FKX / 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.

• Bags, Wraps & Tubing

• Bathing Caps

• Batteries & Battery Assemblies for Infusion Pumps

• Biphasic Defibrillators

• 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 Administration Kit

• Blood Bags For Dialysis

• Blood Bank Supplies (FDA Code: KSS / 864.9050) Blood bank supplies are general purpose devices intended for in vitro use in blood banking. This generic type of device includes products such as blood bank pipettes, blood grouping slides, blood typing tubes, blood typing racks, and cold packs for antisera reagents. The device does not include articles that are licensed by the Center for Biologics Evaluation and Research of the Food and Drug Administration.

• Blood Collect Tubes

• Blood Collection Needles

• Blood Transfusion Sets (FDA Code: BRZ / 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.

• Brush Biopsy Sets

• Buret Administration Intravenous Kit

• Bypass Catheters

• Calcium Compound Bone Void Filler (FDA Code: MQV / 888.3045) A resorbable calcium salt bone void filler device is a resorbable implant intended to fill bony voids or gaps of the extremities, spine, and pelvis that are caused by trauma or surgery and are not intrinsic to the stability of the bony structure.

• Cannula Fistula Needle

• Caps

• Cardiac Catheters

• Cardiac Defibrillators

• Cardiovascular Equipment Kits

• Cardiovascular Patch

• Cardiovascular Procedure Kit (FDA Code: OEZ / 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.

• Cardiovascular Systems

• Cardiovasculars