Profile: Respironics, Inc is a resource for respiratory medical devices. We focus on the diagnosis and treatment of sleep disorders. Our 920M plus handheld pulse oximeter provides on-the-spot blood oximetry and heart rate readings that feature a bigger display, better performance and a 72-hour memory. Our PDx portable diagnostic recording device is intended for obstructive sleep apnea screening, follow-up and diagnostic assessment of cardio-respiratory sleep disorders. The flexible and portable system incorporates advanced features. It satisfies the portable testing requirements for levels II, III and IV and provides capabilities of basic screening to advanced diagnostic evaluation. The PDx enables patients to be tested outside of the lab without compromising study results and helps clinicians avoid the costs associated with retesting.
The company was founded in 1976, has ~20 employees and is ISO 9002, CE certified. NASDAQ:RESP (SEC Filings)
• Sleep Assessment Device (FDA Code: LEL / 882.5050) |
• Sleep Capnographs |
• Sleep Diagnostics Kits, Movement Detection |
• Sleep Disorder Diagnostic Equipment |
• Sleep Disorder Pharmacology Service |
• Sleep Disorder Treatment Marketing Service |
• Sleep-patient Management Software |
• Soft Tip Reusable Pulse Oximeter Sensor |
• Spirometer & Respiratory Aids |
• Spirometers |
• Spirometry Peak Flow Meter (FDA Code: BZH / 868.1860) A peak-flow meter for spirometry is a device used to measure a patient's maximum ventilatory flow rate. |
• Spo2 Pulse Oximeter |
• Stationary Oxygen Concentrators |
• Surgical Masks (FDA Code: FXX / 878.4040) Surgical apparel are devices that are intended to be worn by operating room personnel during surgical procedures to protect both the surgical patient and the operating room personnel from transfer of microorganisms, body fluids, and particulate material. Examples include surgical caps, hoods, masks, gowns, operating room shoes and shoe covers, and isolation masks and gowns. Surgical suits and dresses, commonly known as scrub suits, are excluded. |
• Tabletop Digital Pulse Oximeter |
• Tee Drain/Water Trap (FDA Code: BYH / 868.5995) A tee drain (water trap) is a device intended to trap and drain water that collects in ventilator tubing during respiratory therapy, thereby preventing an increase in breathing resistance. |
• Telemetry Systems |
• Temperature Monitors |
• Test Equipment & Biomedical Devices |
• Therapeutic Incentive Spirometer (FDA Code: BWF / 868.5690) An incentive spirometer is a device that indicates a patient's breathing volume or flow and that provides an incentive to the patient to improve his or her ventilation. |
• Time Cycled Ventilator |
• Tracheostomy Tube with/without Connector (FDA Code: BTO / 868.5800) A tracheostomy tube and tube cuff is a device intended to be placed into a surgical opening of the trachea to facilitate ventilation to the lungs. The cuff may be a separate or integral part of the tracheostomy tube and is, when inflated, intended to establish a seal between the tracheal wall and the tracheostomy tube. The cuff is used to prevent the patient's aspiration of substances, such as blood or vomit, or to provide a means for positive-pressure ventilation of the patient. This device is made of either stainless steel or plastic. |
• Transcutaneous Carbon Dioxide & Oxygen Monitors |
• Transcutaneous Monitors |
• Trend Long-Term Recorder |
• Tubing |
• Unit-dose Respiratory Medication Kits |
• Universal Y Adapter w/flushing Port |
• Used Pulse Oximeters |
• Ventilators |
• Ventilators & Respiratory Therapy Devices |
• Ventilatory Effort Recorder (FDA Code: MNR / 868.2375) A breathing (ventilatory) frequency monitor is a device intended to measure or monitor a patient's respiratory rate. The device may provide an audible or visible alarm when the respiratory rate, averaged over time, is outside operator settable alarm limits. This device does not include the apnea monitor classified in 868.2377. |
• Volume Ventilator |
• Y Adapter (FDA Code: FJP / 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. |
• Y Piece Breathing Circuit (FDA Code: CAI / 868.5240) An anesthesia breathing circuit is a device that is intended to administer medical gases to a patient during anesthesia. It provides both an inhalation and exhalation route and may include a connector, adaptor, and Y-piece. |