Drägerwerk AG & Co. KGaA

Web: http://www.draeger.com
Address: Moislinger Allee 53-55, Lübeck D-23542, Germany
Phone: +49-(0)-451-882-0 | Fax: +49-(0)-451-882-2080 | Map/Directions >>

Profile: Drägerwerk AG & Co. KGaA develops, manufactures & distributes products, integrated solutions & services for acute patient care & home care. Our monitor supports & protects vital human functions, thus creating better and safer conditions for health & the environment. We offer products such as medical therapy devices, medical monitoring, medical architectural systems & light, clinical consumables & accessories. Our services include training in hospital, medical gas management, clinical IT & software solution. We also offer OEM products & components. We also provide anesthesia, critical care unit, neonatal care, fire & emergency services. Our CareArea™ solution for perinatal care is a family-centered solution, which focuses on the seamless integration of information and medical systems. Our product range covers anesthesia workstations, ventilation equipment for intensive and home care, emergency & mobile ventilation units, warming therapy equipment for infants, patient monitoring equipment, IT solutions and gas management systems.

The company was founded in 1889, has revenues of USD 1-5 Million, has ~40 employees.

FDA Registration Number: 9611500
US Agent: Beth Zis / Draeger Medical Systems, Inc.
Phone: +1-(978)-379-8265 Fax: +1-(978)-379-8335 E-Mail:

47 Products/Services (Click for related suppliers)

• Anesthesia Gas-Machine (FDA Code: BSZ / 868.5160)

A gas machine for anesthesia is a device used to administer to a patient, continuously or intermittently, a general inhalation anesthetic and to maintain a patient's ventilation. The device may include a gas flowmeter, vaporizer, ventilator, breathing circuit with bag, and emergency air supply.

• Anesthetic Gas Mask (FDA Code: BSJ / 868.5550)

An anesthetic gas mask is a device, usually made of conductive rubber, that is positioned over a patient's nose or mouth to direct anesthetic gases to the upper airway.

• Bariatric Manual Wheelchairs

• Bicycle Exerciser

• Blood pressure Cuffs (FDA Code: DXQ / 870.1120)

A blood pressure cuff is a device that has an inflatable bladder in an inelastic sleeve (cuff) with a mechanism for inflating and deflating the bladder. The cuff is used in conjunction with another device to determine a subject's blood pressure.

• Breathing Circuit Bacterial Filter (FDA Code: CAH / 868.5260)

A breathing circuit bacterial filter is a device that is intended to remove microbiological and particulate matter from the gases in the breathing circuit.

• Breathing Systems & Accessories

• Carbon-Dioxide Absorbent (FDA Code: CBL / 868.5300)

A carbon dioxide absorbent is a device intended for medical purposes that consists of an absorbent material (e.g., soda lime) that is intended to remove carbon dioxide from the gases in the breathing circuit.

• Continuous Ventilator (FDA Code: CBK / 868.5895)

A continuous ventilator (respirator) is a device intended to mechanically control or assist patient breathing by delivering a predetermined percentage of oxygen in the breathing gas. Adult, pediatric, and neonatal ventilators are included in this generic type of device.

• Disabled/Handicapped Manual Wheelchair (FDA Code: IOR / 890.3850)

A mechanical wheelchair is a manually operated device with wheels that is intended for medical purposes to provide mobility to persons restricted to a sitting position.

• Extension Airway Connector (FDA Code: BZA / 868.5810)

An airway connector is a device intended to connect a breathing gas source to a tracheal tube, tracheostomy tube, or mask.

• 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 Carbon-Dioxide Gas Analyzer (FDA Code: CCK / 868.1400)

A carbon dioxide gas analyzer is a device intended to measure the concentration of carbon dioxide in a gas mixture to aid in determining the patient's ventilatory, circulatory, and metabolic status. The device may use techniques such as chemical titration, absorption of infrared radiation, gas chromatography, or mass spectrometry.

• 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.

• Gaseous Phase Halothane Gas Analyzer (FDA Code: CBS / 868.1620)

A halothane gas analyzer is a device intended to measure the concentration of halothane anesthetic in a gas mixture. The device may use techniques such as mass spectrometry or absorption of infrared or ultraviolet radiation.

• Gaseous Phase Nitrous-Oxide Gas Analyzer (FDA Code: CBR / 868.1700)

A nitrous oxide gas analyzer is a device intended to measure the concentration of nitrous oxide anesthetic in a gas mixture. The device may use techniques such as infrared absorption or mass spectrometry.

• Gaseous-Phase (Anesthetic Concentration) Desflurane Gas Analyzer (FDA Code: NHO / 868.1500)

• Gaseous-Phase (Anesthetic Concentration) Isoflurane Gas Analyzer (FDA Code: NHQ / 868.1500)

• Gaseous-Phase (Anesthetic Concentration) Sevoflurane Gas Analyzer (FDA Code: NHP / 868.1500)

• Handicapped/Physical Therapy Equipment

• Heat and Moisture Condenser (FDA Code: BYD / 868.5375)

A heat and moisture condenser (artificial nose) is a device intended to be positioned over a tracheotomy (a surgically created opening in the throat) or tracheal tube (a tube inserted into the trachea) to warm and humidify gases breathed in by a patient.

• Infant Radiant Warmer (FDA Code: FMT / 880.5130)

The infant radiant warmer is a device consisting of an infrared heating element intended to be placed over an infant to maintain the infant's body temperature by means of radiant heat. The device may also contain a temperature monitoring sensor, a heat output control mechanism, and an alarm system (infant temperature, manual mode if present, and failure alarms) to alert operators of a temperature condition over or under the set temperature, manual mode time limits, and device component failure, respectively. The device may be placed over a pediatric hospital bed or it may be built into the bed as a complete unit.

• Integrated Anesthesia Machines

• Manual Wheelchairs

• Mechanical Wheelchair (FDA Code: IOR / 890.3850)

• MRI Compatible

• Neonatal Incubators (FDA Code: FMZ / 880.5400)

A neonatal incubator is a device consisting of a rigid boxlike enclosure in which an infant may be kept in a controlled environment for medical care. The device may include an AC-powered heater, a fan to circulate the warmed air, a container for water to add humidity, a control valve through which oxygen may be added, and access ports for nursing care.

• Neonatal Incubators (FDA Code: FMZ / 880.5400)

• 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.

• Non-Heated Anesthesia Vaporizer (FDA Code: CAD / 868.5880)

An anesthetic vaporizer is a device used to vaporize liquid anesthetic and deliver a controlled amount of the vapor to the patient.

• Oximeters (FDA Code: DQA / 870.2700)

An oximeter is a device used to transmit radiation at a known wavelength(s) through blood and to measure the blood oxygen saturation based on the amount of reflected or scattered radiation. It may be used alone or in conjunction with a fiberoptic oximeter catheter.

• 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.

• Patient Monitoring Systems

• Patient Physiological Monitor (FDA Code: MHX / 870.1025)

The arrhythmia detector and alarm device monitors an electrocardiogram and is designed to produce a visible or audible signal or alarm when atrial or ventricular arrhythmia, such as premature contraction or ventricular fibrillation, occurs.

• Physiological Monitors Network and Communication System (FDA Code: MSX / 870.2300)

A cardiac monitor (including cardiotachometer and rate alarm) is a device used to measure the heart rate from an analog signal produced by an electrocardiograph, vectorcardiograph, or blood pressure monitor. This device may sound an alarm when the heart rate falls outside preset upper and lower limits.

• Portable Air Compressor (FDA Code: BTI / 868.6250)

A portable air compressor is a device intended to provide compressed air for medical purposes, e.g., to drive ventilators and other respiratory devices.

• Positive End Expiratory Pressure Breathing Attachment (FDA Code: BYE / 868.5965)

A positive end expiratory pressure (PEEP) breathing attachment is a device attached to a ventilator that is used to elevate pressure in a patient's lungs above atmospheric pressure at the end of exhalation.

• Rehabilitation Chair

• Reservoir Bag (FDA Code: BTC / 868.5320)

A reservoir bag is a device, usually made of conductive rubber, intended for use in a breathing circuit as a reservoir for breathing gas and to assist, control, or monitor a patient's ventilation.

• Skin Pressure Protector (FDA Code: FMP / 880.6450)

A skin pressure protector is a device intended for medical purposes that is used to reduce pressure on the skin over a bony prominence to reduce the likelihood of the patient's developing decubitus ulcers (bedsores).

• Surgical Lamps (FDA Code: FTD / 878.4580)

A surgical lamp (including a fixture) is a device intended to be used to provide visible illumination of the surgical field or the patient.

• Surgical Lights (FDA Code: FTD / 878.4580)

• 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.

• 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.

• Wall Vacuum-Powered Operating Room Suction Apparatus (FDA Code: GCX / 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).

• Water Circulating Hot/Cold Pack (FDA Code: ILO / 890.5720)

A water circulating hot or cold pack is a device intended for medical purposes that operates by pumping heated or chilled water through a plastic bag and that provides hot or cold therapy for body surfaces.

• 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.