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Vidacare Corporation


Contact: Robert Titkemeyer
Web: http://www.vidacare.com
Address: 4350 lockhill selma rd,suite 150, shavano park, Texas 78249, USA
Phone: +1-(210)-3758537, 800 680 4911 | Fax: +1-(210)-3758537 | Map/Directions >>
 
 

Profile: Vidacare Corporation has developed a technology platform that has utility across a broad spectrum of medical specialties for both therapeutic and diagnostic purposes. The technology allows clinicians to access the interior of bones (the intraosseous space) quickly and relatively painlessly via the most significant design advance in decades- incorporating simplicity, efficacy, patient comfort, and cost effectiveness. Our products include EZ-IO product system which is an emergency vascular access tool and oncontrolT which brings a new level of technology to bone marrow procedures, minimizing time, pain and effort.

11 Products/Services (Click for related suppliers)  
• Biopsy Instruments (FDA Code: KNW / 876.1075)
A gastroenterology-urology biopsy instrument is a device used to remove, by cutting or aspiration, a specimen of tissue for microscopic examination. This generic type of device includes the biopsy punch, gastrointestinal mechanical biopsy instrument, suction biopsy instrument, gastro-urology biopsy needle and needle set, and nonelectric biopsy forceps. This section does not apply to biopsy instruments that have specialized uses in other medical specialty areas and that are covered by classification regulations in other parts of the device classification regulations.
• Biopsy Instruments (FDA Code: KNW / 876.1075)
• Biopsy Needle Kit (FDA Code: FCG / 876.1075)
• Disposable Needle Set
• Gastrointestinal Mechanical Biopsy Instrument (FDA Code: FCF / 876.1075)
• Intraosseous Infusion System
• Intravenous Administration Kit (FDA Code: FPA / 880.5440)
An intravascular administration set is a device used to administer fluids from a container to a patient's vascular system through a needle or catheter inserted into a vein. The device may include the needle or catheter, tubing, a flow regulator, a drip chamber, an infusion line filter, an I.V. set stopcock, fluid delivery tubing, connectors between parts of the set, a side tube with a cap to serve as an injection site, and a hollow spike to penetrate and connect the tubing to an I.V. bag or other infusion fluid container.
• Rechargeable Replacement Battery (FDA Code: MOQ / 878.4820)
Surgical instrument motors and accessories are AC-powered, battery-powered, or air-powered devices intended for use during surgical procedures to provide power to operate various accessories or attachments to cut hard tissue or bone and soft tissue. Accessories or attachments may include a bur, chisel (osteotome), dermabrasion brush, dermatome, drill bit, hammerhead, pin driver, and saw blade.
• Reusable Aspiration and Injection Needle (FDA Code: GDM / 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.
• Single Lumen Hypodermic Needle (FDA Code: FMI / 880.5570)
A hypodermic single lumen needle is a device intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin. The device consists of a metal tube that is sharpened at one end and at the other end joined to a female connector (hub) designed to mate with a male connector (nozzle) of a piston syringe or an intravascular administration set.
• Vertebroplasty (Does Not Contain Cement) Injector (FDA Code: OAR / 888.4200)
A cement dispenser is a nonpowered syringe-like device intended for use in placing bone cement (888.3027) into surgical sites.

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