Boehringer Laboratories Inc.

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Web: http://www.boehringerlabs.com
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Address: PO Box 870, 500 East Washington St, Norristown, Pennsylvania 19404, USA
Phone: +1-(610)-278-0900 | Fax: +1-(610)-278-0907 | Map/Directions >>

Profile: Boehringer Laboratories Inc. is an ISO 9001 certified medical instrument manufacturer. We specialize in the production of suction regulators, autologous blood processing systems and anesthesia products. Our 3700 series suction regulators are designed to be used in the recovery room, operating room, intensive care unit and patient bedside for intermediate levels of suction, as well as for full line vacuum. Our accessory line includes peak flow meter, bronchodilator tee, arm restraint straps, isolation valve and scavenging pop-off valve. Our model 5300 nitric oxide scavenger-vacuum safety interface features a safe automatic relief of positive and negative pressure, a ventilator adapter, and a 19 mm hose provided with tee to connect to pop-off ventilator.

The company was founded in 1972, has revenues of USD 1-5 Million, has ~30 employees and is ISO 9001, CE certified.

FDA Registration Number: 2518417

46 Products/Services (Click for related suppliers)

• AC-Powered Portable Ward Use Suction Apparatus (FDA Code: JCX / 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.

• Anesthesia Equipment

• Autotransfusion Apparatus (FDA Code: CAC / 868.5830)

An autotransfusion apparatus is a device used to collect and reinfuse the blood lost by a patient due to surgery or trauma.

• Autotransfusion System

• Collecting Vessel Gas (FDA Code: KGK / 868.1575)

A gas collection vessel is a container-like device intended to collect a patient's exhaled gases for subsequent analysis. It does not include a sampling pump.

• Diagnostic Spirometer (FDA Code: BZG / 868.1840)

A diagnostic spirometer is a device used in pulmonary function testing to measure the volume of gas moving in or out of a patient's lungs.

• 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.

• Electric Therapeutic Massager (FDA Code: ISA / 890.5660)

A therapeutic massager is an electrically powered device intended for medical purposes, such as to relieve minor muscle aches and pains.

• General Surgical Aids

• General Surgical Instruments

• Hospital Grade Power Cabels

• Incentive Spirometers

• Inspiratory Airway Pressure Meter (FDA Code: BXR / 868.1780)

An inspiratory airway pressure meter is a device used to measure the amount of pressure produced in a patient's airway during maximal inspiration.

• Inspiratory Force Meters

• Instruments surgical

• Intraoperative Tools

• Manometers

• Mechanical Ventilation, Peep Valves

• Monitoring Spirometer (FDA Code: BZK / 868.1850)

A monitoring spirometer is a device used to measure continuously a patient's tidal volume (volume of gas inhaled by the patient during each respiration cycle) or minute volume (the tidal volume multiplied by the rate of respiration for 1 minute) for the evaluation of the patient's ventilatory status.

• Nasal Inhaler (FDA Code: KCO / 874.5220)

An ear, nose, and throat drug administration device is one of a group of ear, nose, and throat devices intended specifically to administer medicinal substances to treat ear, nose, and throat disorders. These instruments include the powder blower, dropper, ear wick, manual nebulizer pump, and nasal inhaler.

• Nitric Oxide Scavenger Vacuum Safety Interface

• 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.

• Peak Flow Meters

• Pediatric Spirometer

• Positive End Expiratory Pressure (PEEP) Valve

• Positive Expiratory Pressure Devices

• Protective Restraint (FDA Code: FMQ / 880.6760)

A protective restraint is a device, including but not limited to a wristlet, anklet, vest, mitt, straight jacket, body/limb holder, or other type of strap, that is intended for medical purposes and that limits the patient's movements to the extent necessary for treatment, examination, or protection of the patient or others.

• Respiratory Magnetic PEEP Valve

• Respiratory Therapy Devices

• Scavenging (Gas Evacuation) Tubing

• Scavenging Pop-Off Valve

• Skin Closure System (FDA Code: MKY / 878.4320)

A removable skin clip is a clip-like device intended to connect skin tissues temporarily to aid healing. It is not absorbable.

• Spirometers

• Spirometry Peak Flow Meter (FDA Code: BZH / 868.1860)

A peak-flow meter for spirometry is a device used to measure a patient's maximum ventilatory flow rate.

• Suction Equipment

• Suction Regulators

• Surgical Equipment

• Surgical Suction Regulator

• Syringe Holder Adapter (FDA Code: IQG / 890.5050)

A daily activity assist device is a modified adaptor or utensil (e.g., a dressing, grooming, recreational activity, transfer, eating, or homemaking aid) that is intended for medical purposes to assist a patient to perform a specific function.

• 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).

• Vacuum Regulator (FDA Code: KDP / 880.6740)

• Wall Vacuum-Powered Operating Room Suction Apparatus (FDA Code: GCX / 880.6740)

• Wrist/Hand Restraint

• 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.