Ambu Inc

Address: 6740 Baymeadow Drive, Glen Burnie, Maryland 21060, USA
Phone: +1-(800)-262-8462 | Fax: +1-(800)-262-8673 | Map/Directions >>

Profile: Ambu Inc develops, produces and markets diagnostic & life-supporting equipment. Our large ambu blue sensor L features highly conductive wet gel and a combination of instant & long-term adhesives for excellent contact & stable signals throughout the monitoring period. Our laryngeal mask reduces the risk of cross contamination and other hazards. Our Ambu SPUR II is designed for manual ventilation of neonates to adults. It has intergrated handle for user comfort and uniform compression. Our cardiac electrodes for neonatology are designed to withstand some of the most demanding conditions in the hospital like high heat and 80% humidity inside an incubator. Even so, our electrodes are gentle on the delicate skin of a premature baby. We also have extremely tiny electrodes for very premature babies up to term, which are also available in radiotranslucent versions.

The company has revenues of USD 50-100 Million, has ~950 employees and is CE certified.

FDA Registration Number: 9612198
US Agent: Sanjayparikh / Ambu, Inc.
Phone: +1-(410)-768-6464  Fax: +1-(410)-760-4907  E-Mail:

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• Adhesive Bandage Strip
• Adhesive Bandages (FDA Code: KGX / 880.5240)
A medical adhesive tape or adhesive bandage is a device intended for medical purposes that consists of a strip of fabric material or plastic, coated on one side with an adhesive, and may include a pad of surgical dressing without a disinfectant. The device is used to cover and protect wounds, to hold together the skin edges of a wound, to support an injured part of the body, or to secure objects to the skin.
• 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).
• Airway Pressure Monitor (FDA Code: CAP / 868.2600)
An airway pressure monitor is a device used to measure the pressure in a patient's upper airway. The device may include a pressure gauge and an alarm.
• Airway Pressure Monitor with Alarm (FDA Code: CAP / 868.2600)
• Airway Pressure Monitor with Gauge (FDA Code: CAP / 868.2600)
• Alternating Pressure Air Flotation Mattress (FDA Code: FNM / 880.5550)
• Anesthesia Equipment
• Anesthesia Equipment
• Anesthesiology Oropharyngeal Airway (FDA Code: CAE / 868.5110)
An oropharyngeal airway is a device inserted into a patient's pharynx through the mouth to provide a patent airway.
• 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.
• Angiographic Catheter, Pigtail Diagnostic Catheters
• Automotive Diagnostic Equipment
• Backboards
• Breathing Frequency Monitor (FDA Code: BZQ / 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.
• Cardiopulmonary Resuscitation Emergency Cart (FDA Code: BZN / 868.6175)
A cardiopulmonary emergency cart is a device intended to store and transport resuscitation supplies for emergency treatment. The device does not include any equipment used in cardiopulmonary resuscitation.
• Cardiopulmonary Resuscitation Emergency Kit
• Cervical Orthosis (FDA Code: IQK / 890.3490)
A truncal orthosis is a device intended for medical purposes to support or to immobilize fractures, strains, or sprains of the neck or trunk of the body. Examples of truncal orthoses are the following: Abdominal, cervical, cervical-thoracic, lumbar, lumbo-sacral, rib fracture, sacroiliac, and thoracic orthoses and clavicle splints.
• Cervical Spine extrication collar
• CLIA-Waived Diagnostic Devices, Microhematocrit Centrifuges
• Clinical Diagnostic Solutions, Hematology Reagents
• Cliplight Diagnostic Lamp
• Computer Softwares
• Connecting Flexible Aspirating Tube (FDA Code: BYY / 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).
• Continuous Positive Airway Pressure Unit
• 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.
• Controls for Diagnostic Equipment
• Corneal and Refractive Diagnostics, Esthesiometers
• Coronary Diagnostic Catheters
• CPR (Resuscitation) Training Manikin
• CPR Assist Device (FDA Code: LYM)
• CPR Equipment
• Cutaneous Electrode (FDA Code: GXY / 882.1320)
A cutaneous electrode is an electrode that is applied directly to a patient's skin either to record physiological signals (e.g., the electroencephalogram) or to apply electrical stimulation.
• Detachable Needle Electrode Cables & Accessories
• Diagnostic Aids
• Diagnostic Angiography
• Diagnostic Catheter
• Diagnostic Catheters Pigtail Ventriculography
• Diagnostic Catheters Pigtail, Aortography
• Diagnostic Catheters, angiography
• Diagnostic Chart, Anatomical
• Diagnostic Charts
• Diagnostic Contact Lenses
• Diagnostic Coronary Sinus EP Catheters
• Diagnostic Cystoscopes
• Diagnostic Devices
• Diagnostic Devices, Stress Test Base Systems
• Diagnostic Dye
• Diagnostic Electromyograph Needle Electrode (FDA Code: IKT / 890.1385)
A diagnostic electromyograph needle electrode is a monopolar or bipolar needle intended to be inserted into muscle or nerve tissue to sense bioelectrical signals. The device is intended for medical purposes for use in connection with electromyography (recording the intrinsic electrical properties of skeletal muscle).
• Diagnostic EP Cables

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