Headstar Medical Products Co., Ltd

Contact: Sunny Liao
Web: http://www.headstarmedical.com
Address: 9 F., No. 8, Sec. 1, Chung-Shan Road, Hsin-Chang, City, Taipei County 242, Taiwan
Phone: +866-(2)-8521-7623 | Fax: +866-(2)--8522-5703 | Map/Directions >>

Profile: Headstar Medical Products Co., Ltd designs, manufactures and sells respiratory therapy products. Our products are manual resuscitator, suction unit, oxygen therapy, aerosol therapy, humidification, face mask, airway management and manometer. Our suction unit is manually powered and is designed to be operated by a person unaided for clearing patient's airway at home or for field use, where there is no electrical power source. It creates negative pressure (vacuum) to draw fluids via disposable tubing which is connected to a collection canister. To ensure that fluids will not overflow, the canister is designed with full stop protection for our selected handheld suction units. Our oxygen therapy products include venturi set, nasal cannula, oxygen tubing, tracheotomy mask and oxygen mask.

The company was founded in 1997 and is ISO 13485, CE certified.

FDA Registration Number: 9616354
US Agent: Tim Juang / Jeco, Inc.
Phone: +1-(909)-563-1600 Fax: +1-(909)-563-1625 E-Mail:

16 Products/Services (Click for related suppliers)

• 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.

• 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.

• 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.

• Mouth Gags (FDA Code: KBN / 874.4420)

• Non-Direct Patient Interface Humidifier (FDA Code: KFZ / 868.5460)

A therapeutic humidifier for home use is a device that adds water vapor to breathing gases and that is intended for respiratory therapy or other medical purposes. The vapor produced by the device pervades the area surrounding the patient, who breathes the vapor during normal respiration.

• 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-Sterile External Non-Inflatable Extremity Splint (FDA Code: NOC / 878.3910)

A noninflatable extremity splint is a device intended to immobilize a limb or an extremity. It is not inflatable.

• Non-Ventilatory Medicinal Nebulizer/Atomizer (FDA Code: CCQ / 868.5640)

A medicinal nonventilatory nebulizer (atomizer) is a device that is intended to spray liquid medication in aerosol form into the air that a patient will breathe.

• 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.

• Oxygen Nasal Cannula (FDA Code: CAT / 868.5340)

A nasal oxygen cannula is a two-pronged device used to administer oxygen to a patient through both nostrils.

• Rigid Laryngoscope (FDA Code: CCW / 868.5540)

A rigid laryngoscope is a device used to examine and visualize a patient's upper airway and aid placement of a tracheal tube.

• Tee Drain/Water Trap (FDA Code: BYH / 868.5995)

A tee drain (water trap) is a device intended to trap and drain water that collects in ventilator tubing during respiratory therapy, thereby preventing an increase in breathing resistance.

• Tracheobronchial Suction Catheter (FDA Code: BSY / 868.6810)

A tracheobronchial suction catheter is a device used to aspirate liquids or semisolids from a patient's upper airway.

• Ventilator Tubing and Support Set (FDA Code: BZO / 868.5975)

Ventilator tubing is a device intended for use as a conduit for gases between a ventilator and a patient during ventilation of the patient.

• Venturi Low Concentration Oxygen Mask (FDA Code: BYF / 868.5600)

A venturi mask is a device containing an air-oxygen mixing mechanism that dilutes 100 percent oxygen to a predetermined concentration and delivers the mixed gases to a patient.

• 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.