Minrad, Inc.

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Contact: Dan McAllister - Vice President
Web: http://www.minrad.com
E-Mail:
Address: 50 Cobham Dr., Orchard Park, New York 14127, USA
Phone: +1-(716)-855-1068, 800-832-3303 | Fax: +1-(716)-855-1078 | Map/Directions >>

Profile: Minrad, Inc. specializes in healthcare products under the categories such as acute care devices and acute care pharmaceuticals. Our product list comprises of syringes, core tissue needles, spinal needles, introducer needles and bone biopsy needles. Our Light Sabre™ products incorporate a patented light collimating tube that works with the SabreSource™ system laser for accurate placement during fluoroscopically-guided surgery and interventional procedures. When properly aligned with the SabreSource™ system laser, the patented Light Sabre™ collimating tube glows brightly, providing an easily seen indication that the device is on target to reach the desired sub-surface anatomy, with an accuracy of +/- 3 mm up to a depth of 100 mm. The Light Sabre™ introducer needle is packaged in a sterile peel-pouch with one collimating tube.

FDA Registration Number: 1320909

20 Products/Services (Click for related suppliers)

• Acute Care Devices

• Anesthesia Inhalation Fluids

• Aspirating Needles

• 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)

• Bone Biopsy Needles

• Core Tissue Needles

• Disposable Surgical Drape (FDA Code: KKX / 878.4370)

A surgical drape and drape accessories is a device made of natural or synthetic materials intended to be used as a protective patient covering, such as to isolate a site of surgical incision from microbial and other contamination. The device includes a plastic wound protector that may adhere to the skin around a surgical incision or be placed in a wound to cover its exposed edges, and a latex drape with a self-retaining finger cot that is intended to allow repeated insertion of the surgeon's finger into the rectum during performance of a transurethral prostatectomy.

• General Surgical Manual Instrument (FDA Code: MDM / 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.

• Image-Intensified Fluoroscopic X-Ray System (FDA Code: JAA / 892.1650)

An image-intensified fluoroscopic x-ray system is a device intended to visualize anatomical structures by converting a pattern of x-radiation into a visible image through electronic amplification. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.

• Light Beam Patient Position Monitor (FDA Code: IWE / 892.5780)

A light beam patient position indicator is a device that projects a beam of light (incoherent light or laser) to determine the alignment of the patient with a radiation beam. The beam of light is intended to be used during radiologic procedures to ensure proper positioning of the patient and to monitor alignment of the radiation beam with the patient's anatomy.

• Piston Syringe (FDA Code: FMF / 880.5860)

A piston syringe is a device intended for medical purposes that consists of a calibrated hollow barrel and a movable plunger. At one end of the barrel there is a male connector (nozzle) for fitting the female connector (hub) of a hypodermic single lumen needle. The device is used to inject fluids into, or withdraw fluids from, the body.

• 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.

• Spinal Needles

• Sterile Surgical Drapes (FDA Code: KKX / 878.4370)

• Surgical Drapes (FDA Code: KKX / 878.4370)

• Surgical Drapes & Packs (FDA Code: KKX / 878.4370)

• Syringes

• Urology Surgical Drapes (FDA Code: KKX / 878.4370)