Air Safety Ltd

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Contact: S Brown
Web: http://www.airsafetymedical.com/Airsafety
E-Mail:
Address: Nfc House, Mellishaw Lane, Morecambe, Lancs LA3 3EN, United Kingdom
Phone: +44-(1524)-388696 | Fax: +44-(1524)-33386 | Map/Directions >>

Profile: Air Safety Ltd is a manufacturer and distributor of air filtration devices. We offer heat and moisture exchanger & filter to use during surgery to ensure that patients airways are humidified and filtered. Our filter range includes bacterial/viral , combined filter heat and moisture exchangers and specialized units. Our product line covers pleated filters, anesthetic face makers, catheter mounts, intensive therapy ventilator protection devices and suction filters. Our mechanical pleated filters carry hydrophobic properties which provide a complete barrier to viral pathogens under normal clinical conditions.

The company is ISO 9001:2000, ISO 13485:2001 certified.

FDA Registration Number: 3004428458
US Agent: Paul Dryden / Promedic, Llc
Phone: +1-(239)-307-6061 Fax: +1-(239)-307-6070 E-Mail:

6 Products/Services (Click for related suppliers)

• 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.

• Continuous Respirator Accessory (FDA Code: MOD / 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.

• Continuous Ventilator Accessory (FDA Code: MOD / 868.5895)

• 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.

• 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.

• 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).