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Firstar Healthcare Co., Ltd.

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Contact: Terry Tan
Web: http://www.china-firstar.com
E-Mail:
Address: No.4-5, 2nd Industrial District, Dong Shen Cun, Dongchong Town ,Panyu District, Guangzhou 511475, China
Phone: +86-(20)-28865699 | Fax: +86-(20)-28865718 | Map/Directions >>
 
 

Profile: Firstar Healthcare Co., Ltd. is an exporter of first aid kits and health care products. Our products include surgical, blood collection, wound care, surgical dressings and home care products. We also supply pressure bandages, tooth whitener & stain eraser, interdental brushes and mini first aid box.

FDA Registration Number: 3003887292
US Agent: Mark R. Harris / Injection Safety Industries, Llc
Phone: +1-(270)-846-7116  Fax: +1-(270)-846-4484  E-Mail:

46 Products/Services (Click for related suppliers)  
• 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.
• Adult Tongue Depressor (FDA Code: FMA / 880.6230)
A tongue depressor is a device intended to displace the tongue to facilitate examination of the surrounding organs and tissues.
• 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.
• Breathing Mouthpiece (FDA Code: BYP / 868.5620)
A breathing mouthpiece is a rigid device that is inserted into a patient's mouth and that connects with diagnostic or therapeutic respiratory devices.
• Cardiopulmonary Resuscitation Aid Kit (FDA Code: OEV / 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.
• Cast Bandage (FDA Code: ITG / 890.3025)
A prosthetic and orthotic accessory is a device intended for medical purposes to support, protect, or aid in the use of a cast, orthosis (brace), or prosthesis. Examples of prosthetic and orthotic accessories include the following: A pelvic support band and belt, a cast shoe, a cast bandage, a limb cover, a prosthesis alignment device, a postsurgical pylon, a transverse rotator, and a temporary training splint.
• Cement Dispenser (FDA Code: KIH / 888.4200)
A cement dispenser is a nonpowered syringe-like device intended for use in placing bone cement (888.3027) into surgical sites.
• Disposable Hot/Cold Pack (FDA Code: IMD / 890.5710)
A hot or cold disposable pack is a device intended for medical purposes that consists of a sealed plastic bag incorporating chemicals that, upon activation, provides hot or cold therapy for body surfaces.
• Disposable Medical Scissors (FDA Code: JOK / 880.6820)
Medical disposable scissors are disposable type general cutting devices intended for medical purposes. This generic type of device does not include surgical scissors.
• Elastic Bandages (FDA Code: FQM / 880.5075)
An elastic bandage is a device consisting of either a long flat strip or a tube of elasticized material that is used to support and compress a part of a patient's body.
• External Inflatable Extremity Splint (FDA Code: FZF / 878.3900)
An inflatable extremity splint is a device intended to be inflated to immobilize a limb or an extremity.
• First Aid Kit Without Drug (FDA Code: OHO / 878.4014)
A nonresorbable gauze/sponge for external use is a sterile or nonsterile device intended for medical purposes, such as to be placed directly on a patient's wound to absorb exudate. It consists of a strip, piece, or pad made from open woven or nonwoven mesh cotton cellulose or a simple chemical derivative of cellulose. This classification does not include a nonresorbable gauze/sponge for external use that contains added drugs such as antimicrobial agents, added biologics such as growth factors, or is composed of materials derived from animal sources.
• Forceps (FDA Code: HTD / 878.4800)
A manual surgical instrument for general use is a nonpowered, hand-held, or hand-manipulated device, either reusable or disposable, intended to be used in various general surgical procedures. The device includes the applicator, clip applier, biopsy brush, manual dermabrasion brush, scrub brush, cannula, ligature carrier, chisel, clamp, contractor, curette, cutter, dissector, elevator, skin graft expander, file, forceps, gouge, instrument guide, needle guide, hammer, hemostat, amputation hook, ligature passing and knot-tying instrument, knife, blood lancet, mallet, disposable or reusable aspiration and injection needle, disposable or reusable suturing needle, osteotome, pliers, rasp, retainer, retractor, saw, scalpel blade, scalpel handle, one-piece scalpel, snare, spatula, stapler, disposable or reusable stripper, stylet, suturing apparatus for the stomach and intestine, measuring tape, and calipers. A surgical instrument that has specialized uses in a specific medical specialty is classified in separate regulations in parts 868 through 892.
• General & Plastic Surgery Biopsy Brush (FDA Code: GEE / 878.4800)
• Hand-Carried Stretcher (FDA Code: FPP / 880.6900)
A hand-carried stretcher is a device consisting of a lightweight frame, or of two poles with a cloth or metal platform, on which a patient can be carried.
• Hydrophilic Wound Dressings (FDA Code: NAC / 878.4018)
A hydrophilic wound dressing is a sterile or non-sterile device intended to cover a wound and to absorb exudate. It consists of nonresorbable materials with hydrophilic properties that are capable of absorbing exudate (e.g., cotton, cotton derivatives, alginates, dextran, and rayon). This classification does not include a hydrophilic wound dressing that contains added drugs such as antimicrobial agents, added biologics such as growth factors, or is composed of materials derived from animal sources.
• Incontinence Protective Garment (FDA Code: EYQ / 876.5920)
A protective garment for incontinence is a device that consists of absorbent padding and a fluid barrier and that is intended to protect an incontinent patient's garment from the patient's excreta. This generic type of device does not include diapers for infants.
• Infant Tongue Depressor (FDA Code: FMA / 880.6230)
• Junior Tongue Depressor (FDA Code: FMA / 880.6230)
• Liquid Crystal Forehead Temperature Strip (FDA Code: KPD / 880.2200)
A liquid crystal forehead temperature strip is a device applied to the forehead that is used to indicate the presence or absence of fever, or to monitor body temperature changes. The device displays the color changes of heat sensitive liquid crystals corresponding to the variation in the surface temperature of the skin. The liquid crystals, which are cholesteric esters, are sealed in plastic.
• Manual Stethoscope (FDA Code: LDE / 870.1875)
A manual stethoscope is a mechanical device used to project the sounds associated with the heart, arteries, and veins and other internal organs.
• Manual Vacuum-Assisted Blood Collect System (FDA Code: KST / 864.9125)
A vacuum-assisted blood collection system is a device intended for medical purposes that uses a vacuum to draw blood for subsequent reinfusion.
• Medication Reminder (FDA Code: NXQ / 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.
• Non-Pneumatic Tourniquet (FDA Code: GAX / 878.5900)
A nonpneumatic tourniquet is a device consisting of a strap or tubing intended to be wrapped around a patient's limb and tightened to reduce circulation.
• 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 Absorbent Tipped Applicator (FDA Code: KXF / 880.6025)
An absorbent tipped applicator is a device intended for medical purposes that consists of an absorbent swab on a wooden, paper, or plastic stick. The device is used to apply medications to, or to take specimens from, a patient.
• Non-Sterile Specimen Container (FDA Code: NNI / 864.3250)
A specimen transport and storage container, which may be empty or prefilled, is a device intended to contain biological specimens, body waste, or body exudate during storage and transport in order that the matter contained therein can be destroyed or used effectively for diagnostic examination. If prefilled, the device contains a fixative solution or other general purpose reagent to preserve the condition of a biological specimen added to the container. This section does not apply to specimen transport and storage containers that are intended for use as part of an over-the-counter test sample collection system for drugs of abuse testing.
• Non-Sterile Specimen Mailer And Storage Container (FDA Code: NNK / 864.3250)
• Non-Surgical Tongue Depressor (FDA Code: FMA / 880.6230)
• Nonresorbable Gauze/sponge for External Use (FDA Code: NAB / 878.4014)
• Ophthalmic Eye Pad (FDA Code: HMP / 878.4440)
An eye pad is a device that consists of a pad made of various materials, such as gauze and cotton, intended for use as a bandage over the eye for protection or absorption of secretions.
• Oval Eye Pads (FDA Code: HMP / 878.4440)
• 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 Catheter (FDA Code: BZB / 868.5350)
A nasal oxygen catheter is a device intended to be inserted through a patient's nostril to administer oxygen.
• Pin Crimper (FDA Code: HXQ / 888.4540)
An orthopedic manual surgical instrument is a nonpowered hand-held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery. This generic type of device includes the cerclage applier, awl, bender, drill brace, broach, burr, corkscrew, countersink, pin crimper, wire cutter, prosthesis driver, extractor, file, fork, needle holder, impactor, bending or contouring instrument, compression instrument, passer, socket positioner, probe, femoral neck punch, socket pusher, reamer, rongeur, scissors, screwdriver, bone skid, staple driver, bone screw starter, surgical stripper, tamp, bone tap, trephine, wire twister, and wrench.
• Reusable Hot /Cold Pack (FDA Code: IME / 890.5700)
A cold pack is a device intended for medical purposes that consists of a compact fabric envelope containing a specially hydrated pliable silicate gel capable of forming to the contour of the body and that provides cold therapy for body surfaces.
• Scavenging Mask (FDA Code: KHA / 868.5590)
A scavenging mask is a device positioned over a patient's nose to deliver anesthetic or analgesic gases to the upper airway and to remove excess and exhaled gas. It is usually used during dentistry.
• Scented-Deodorized Menstrual Pads (FDA Code: NRC / 884.5425)
A scented or scented deodorized menstrual pad is a device that is a pad made of cellulosic or synthetic material which is used to absorb menstrual or other vaginal discharge. It has scent (i.e., fragrance materials) added for aesthetic purposes (scented menstrual pad) or for deodorizing purposes (scented deodorized menstrual pad). This generic type of device includes sterile scented menstrual pads used for medically indicated conditions, but does not include menstrual pads treated with added antimicrobial agents or other drugs.
• Skin Pressure Protector (FDA Code: FMP / 880.6450)
A skin pressure protector is a device intended for medical purposes that is used to reduce pressure on the skin over a bony prominence to reduce the likelihood of the patient's developing decubitus ulcers (bedsores).
• Sterile Closed Urine Drainage System for Nonindwelling Catheter (FDA Code: EYZ / 876.5250)
A urine collector and accessories is a device intended to collect urine. The device and accessories consist of tubing, a suitable receptacle, connectors, mechanical supports, and may include a means to prevent the backflow of urine or ascent of infection. The two kinds of urine collectors are:
• Suction Catheter and Tip (FDA Code: JOL / 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).
• Surgical Caps (FDA Code: FYF / 878.4040)
Surgical apparel are devices that are intended to be worn by operating room personnel during surgical procedures to protect both the surgical patient and the operating room personnel from transfer of microorganisms, body fluids, and particulate material. Examples include surgical caps, hoods, masks, gowns, operating room shoes and shoe covers, and isolation masks and gowns. Surgical suits and dresses, commonly known as scrub suits, are excluded.
• Tongue Depressors (FDA Code: FMA / 880.6230)
• Vinyl Patient Examination Glove (FDA Code: LYZ / 880.6250)
A patient examination glove is a disposable device intended for medical purposes that is worn on the examiner's hand or finger to prevent contamination between patient and examiner.
• X-Ray Detectable Gauze (FDA Code: GDY / 878.4450)
Nonabsorbable gauze for internal use is a device made of an open mesh fabric intended to be used inside the body or a surgical incision or applied to internal organs or structures, to control bleeding, absorb fluid, or protect organs or structures from abrasion, drying, or contamination. The device is woven from material made of not less than 50 percent by mass cotton, cellulose, or a simple chemical derivative of cellulose, and contains x-ray detectable elements.

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