Ambu A/s

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Contact: Lars Marcher - President & CEO
Web: http://www.ambu.com
E-Mail:
Address: Baltorpbakken 13, Ballerup DK-2750, Denmark
Phone: +45-(7225)-2000 | Fax: +45-(7225)-2050 | Map/Directions >>

Profile: Ambu A/s develops and produces diagnostic equipments. Our Ambu® oxygen regulators are designed to deliver precise pressure regulation of oxygen for medium-flow applications using resuscitators. Our Ambu® TubeChek is a device which is used to confirm the placement of endotracheal tube. Our Ambu® disposable face masks are designed for the manual & automatic resuscitators and ventilators.

FDA Registration Number: 9610691
US Agent: Sanjay Parikh / Ambu Inc.
Phone: +1-(410)-768-6464 Fax: +1-(410)-760-4907 E-Mail:

12 Products/Services (Click for related suppliers)

• Air Flotation Mattress (FDA Code: FNM / 880.5550)

An alternating pressure air flotation mattress is a device intended for medical purposes that consists of a mattress with multiple air cells that can be filled and emptied in an alternating pattern by an associated control unit to provide regular, frequent, and automatic changes in the distribution of body pressure. The device is used to prevent and treat decubitus ulcers (bed sores).

• Alternating Pressure Air Flotation Mattress (FDA Code: FNM / 880.5550)

• Manual Emergency Ventilator/Resuscitator (FDA Code: BTM / 868.5915)

A manual emergency ventilator is a device, usually incorporating a bag and valve, intended to provide emergency respiratory support by means of a face mask or a tube inserted into a patient's airway.

• Manual/Powered Portable Aspiration Pump (FDA Code: BTA / 878.4780)

A powered suction pump is a portable, AC-powered or compressed air-powered device intended to be used to remove infectious materials from wounds or fluids from a patient's airway or respiratory support system. The device may be used during surgery in the operating room or at the patient's bedside. The device may include a microbial filter.

• Non-Powered Portable Single Patient Suction Apparatus (FDA Code: GCY / 878.4680)

A nonpowered, single patient, portable suction apparatus is a device that consists of a manually operated plastic, disposable evacuation system intended to provide a vacuum for suction drainage of surgical wounds.

• Non-Rebreathing Oxygen Mask (FDA Code: KGB / 868.5570)

A nonrebreathing mask is a device fitting over a patient's face to administer oxygen. It utilizes one-way valves to prevent the patient from rebreathing previously exhaled gases.

• 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.

• 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.

• 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.

• 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.

• Tracheal Tube with/without Connector (FDA Code: BTR / 868.5730)

A tracheal tube is a device inserted into a patient's trachea via the nose or mouth and used to maintain an open airway.

• Vacuum Collection Bottle (FDA Code: KDQ / 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).