Profile: Smiths Medical ASD, Inc supplies devices that are used during critical & intensive care, surgery, post-operative care during recovery & in a series of high-end home infusion therapies. We focus on developing technologies that offer both clinical & economic advantages to our healthcare providers and patients. We render market-leading solutions in anaesthesia & safety devices. Our Venipuncture Needle-Pro® device is a holder-based safety device that minimizes back-end exposure by preventing needle removal and holder re-use & is compliant with OSHA directives.

The company was founded in 1978, has revenues of USD 25-50 Million, has ~280 employees and is ISO 9001, CE certified. LON:SMIN (SEC Filings)

FDA Registration Number: 1824231

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• Combined Spinal Epidural System

• Compact Anesthesia Monitor

• Conmed Electrosurgery

• 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 Catheter Flush Valve

• Continuous Electronic Thermometer (FDA Code: FLL / 880.2910) A clinical electronic thermometer is a device used to measure the body temperature of a patient by means of a transducer coupled with an electronic signal amplification, conditioning, and display unit. The transducer may be in a detachable probe with or without a disposable cover.

• Continuous Flush Catheter (FDA Code: KRA / 870.1210) A continuous flush catheter is an attachment to a catheter-transducer system that permits continuous intravascular flushing at a slow infusion rate for the purpose of eliminating clotting, back-leakage, and waveform damping.

• Contract Manufacturing

• CPR Equipment

• Cricothyrotomy Kits (FDA Code: OGP / 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.

• Cuff Monitoring Systems

• Cuff Pressure Monitor

• Custom Tubing Clamp

• 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.

• Differential Ventilation Tracheal/Bronchial Tube (FDA Code: CBI / 868.5740) A tracheal/bronchial differential ventilation tube is a device used to isolate the left or the right lung of a patient for anesthesia or pulmonary function testing.

• Digital Pulse Oximeter

• Direct Patient Interface Nebulizer (FDA Code: CAF / 868.5630) A nebulizer is a device intended to spray liquids in aerosol form into gases that are delivered directly to the patient for breathing. Heated, ultrasonic, gas, venturi, and refillable nebulizers are included in this generic type of device.

• Direct Patient Interface Respiratory Gas Humidifier (FDA Code: BTT / 868.5450) A respiratory gas humidifier is a device that is intended to add moisture to, and sometimes to warm, the breathing gases for administration to a patient. Cascade, gas, heated, and prefilled humidifiers are included in this generic type of device.

• Disposable Adult Finger Sensor

• Disposable Infant Finger Sensor

• Disposable Needles

• Disposable Neonate Finger Sensor

• Disposable Normothermic IV Accessories

• Disposable Normothermic IV Administration Sets

• Disposable Pediatric Finger Sensor

• Disposable Product Contract Manufacturing

• Disposable Surgical scalpels

• Disposable Syringes

• Disposables Ambulatory Pump

• Disposbale Pulse Oximeter Sensors

• Double and Triple Head Stethoscopes

• Dry Lithium Heparin

• Ear Oximeter (FDA Code: DPZ / 870.2710) An ear oximeter is an extravascular device used to transmit light at a known wavelength(s) through blood in the ear. The amount of reflected or scattered light as indicated by this device is used to measure the blood oxygen saturation.

• ECG Monitor

• ECG Monitoring Electrodes

• ECG Monitors Service

• Electrosurgery

• Emergency Airway Needle (FDA Code: BWC / 868.5090) An emergency airway needle is a device intended to puncture a patient's cricothyroid membrane to provide an emergency airway during upper airway obstruction.

• Emergency Care Supplies

• Emergency Cricothyrotomy Kit

• Endotracheal Tubes

• Endotracheal Tubes, Close Fitting

• Endotracheal Tubes, High Volume Tapered

• ENT Tracheostomy Tube

• Esophageal Stethoscopes with Temperature

• Event ECG Monitors

• 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.

• Female External Urethral Occluder (FDA Code: MNG / 876.5160) A urological clamp for males is a device used to close the urethra of a male to control urinary incontinence or to hold anesthetic or radiography contrast media in the urethra temporarily. It is an external clamp.

• Female Incontinence Implant

• Fetal Pulse Oximeter (FDA Code: MMA)