Profile: Fisher & Paykel Healthcare designs, manufactures and markets heated humidification devices used in respiratory care & in the treatment of obstructive sleep apnea. We are an ISO 9001 & CE MARK certified company. We offer products for obstructive sleep apnea, respiratory humidification & neonatal. The product neonatal offers infant warming, infant resuscitation & respiratory support. The infant warmer rewarms and stabilizes the newborn baby immediately after delivery. The integrated bassinet and optional accessories offer convenient and easy-to-use equipment for optimal thermal care and resuscitation. Our Neopuff™ infant resuscitator is an easy to use, manually operated, gas-powered resuscitator that provides optimal resuscitation. Our HC150 with ambient tracking® renders humidification benefits of our integrated sleepstyle™ 200 series.

The company has ~300 employees and is ISO 9001, CE certified.

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• Neonatal Phototherapy Equipment

• Neonatal Phototherapy Unit (FDA Code: LBI / 880.5700) A neonatal phototherapy unit is a device used to treat or prevent hyperbilirubinemia (elevated serum bilirubin level). The device consists of one or more lamps that emit a specific spectral band of light, under which an infant is placed for therapy. This generic type of device may include supports for the patient and equipment and component parts.

• Nerve Stimulators

• Non-Continuous Ventilator/Respirator (FDA Code: BZD / 868.5905) A noncontinuous ventilator (intermittent positive pressure breathing-IPPB) is a device intended to deliver intermittently an aerosol to a patient's lungs or to assist a patient's breathing.

• Non-Rebreathing Valve (FDA Code: CBP / 868.5870) A nonrebreathing valve is a one-way valve that directs breathing gas flow to the patient and vents exhaled gases into the atmosphere.

• Obstructive Sleep Apnea (OSA) Treatment

• Oral Mask

• OSHA Compliance Training

• Oxygen Masks (FDA Code: BYG / 868.5580) An oxygen mask is a device placed over a patient's nose, mouth, or tracheostomy to administer oxygen or aerosols.

• Oxygen Nasal Cannula (FDA Code: CAT / 868.5340) A nasal oxygen cannula is a two-pronged device used to administer oxygen to a patient through both nostrils.

• Oxygen Therapy, Oxygen Cannulae

• Passover Humidifiers

• Patient Scale (FDA Code: FRW / 880.2720) A patient scale is a device intended for medical purposes that is used to measure the weight of a patient who cannot stand on a scale. This generic device includes devices placed under a bed or chair to weigh both the support and the patient, devices where the patient is lifted by a sling from a bed to be weighed, and devices where the patient is placed on the scale platform to be weighed. The device may be mechanical, battery powered, or AC-powered and may include transducers, electronic signal amplification, conditioning and display equipment.

• Peripheral Electric Nerve Stimulator (FDA Code: KOI / 868.2775) An electrical peripheral nerve stimulator (neuromuscular blockade monitor) is a device used to apply an electrical current to a patient to test the level of pharmacological effect of anesthetic drugs and gases.

• Peripheral Nerve Stimulators

• Portable Oxygen Generator (FDA Code: CAW / 868.5440) A portable oxygen generator is a device that is intended to release oxygen for respiratory therapy by means of either a chemical reaction or physical means (e.g., a molecular sieve).

• Positive Airway Pressure Therapy (CPAP) Systems

• Positive Airway Pressure Therapy, Cannulae

• Positive Airway Pressure Therapy, Headgear

• Positive Airway Pressure Therapy, Masks

• Powered Emergency Ventilator/Resuscitator (FDA Code: BTL / 868.5925) A powered emergency ventilator is a demand valve or inhalator intended to provide emergency respiratory support by means of a face mask or a tube inserted into a patient's airway.

• Pressure Tubing and Accessories (FDA Code: BYX / 868.5860) Pressure tubing and accessories are flexible or rigid devices intended to deliver pressurized medical gases.

• Respiratory Humidifiers

• Respiratory Products, CPAP Units

• Resuscitation

• Resuscitation Equipment

• Seminar Service

• Sleep Diagnostic Lab Kits

• 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.

• 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.

• Therapeutic Heating Infrared Lamp (FDA Code: ILY / 890.5500) An infrared lamp is a device intended for medical purposes that emits energy at infrared frequencies (approximately 700 nanometers to 50,000 nanometers) to provide topical heating.

• TInfrared Light (FDA Code: ILY / 890.5500)

• Tubing

• Vacuum Regulator (FDA Code: KDP / 880.6740) A vacuum-powered body fluid suction apparatus is a device used to aspirate, remove, or sample body fluids. The device is powered by an external source of vacuum. This generic type of device includes vacuum regulators, vacuum collection bottles, suction catheters and tips, connecting flexible aspirating tubes, rigid suction tips, specimen traps, noninvasive tubing, and suction regulators (with gauge).

• Vagal Nerve Stimulators

• Ventilator Tubing and Support Set (FDA Code: BZO / 868.5975) Ventilator tubing is a device intended for use as a conduit for gases between a ventilator and a patient during ventilation of the patient.

• Ventilators

• Venturi Low Concentration Oxygen Mask (FDA Code: BYF / 868.5600) A venturi mask is a device containing an air-oxygen mixing mechanism that dilutes 100 percent oxygen to a predetermined concentration and delivers the mixed gases to a patient.

• 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.