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Arrow Internacional De Mexico, S.A. De C.V.


Address: Modulo 1, Circuito 5, Parque Industrias De America, Col. Panamericana, Chihuahua 31200, Mexico
Phone: +52-(610)-378-0131 | Map/Directions >>
 
 

Profile: Arrow Internacional De Mexico, S.A. De C.V. offers multiple sterile needleless injection hub, wire guides and various intravascular catheters.

FDA Registration Number: 9680794
US Agent: Kenneth Oshansky / Arrow International, Inc. (subsidiary Of Teleflex, Inc.)
Phone: +1-(610)-413-7665  E-Mail:

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• 2nd Antibody Sep. Goat Antibody Digoxin (3-H) Radioimmunoassay (FDA Code: DOY / 862.3320)
A digoxin test system is a device intended to measure digoxin, a cardiovascular drug, in serum and plasma. Measurements obtained by this device are used in the diagnosis and treatment of digoxin overdose and in monitoring levels of digoxin to ensure appropriate therapy.
• Anesthesia Conduction Kit (FDA Code: CAZ / 868.5140)
An anesthesia conduction kit is a device used to administer to a patient conduction, regional, or local anesthesia. The device may contain syringes, needles, and drugs.
• Anesthetic Conduction Needle with/without Introducer (FDA Code: BSP / 868.5150)
An anesthesia conduction needle is a device used to inject local anesthetics into a patient to provide regional anesthesia.
• Atherectomy Peripheral Catheter (FDA Code: MCW / 870.4875)
An intraluminal artery stripper is a device used to perform an endarterectomy (removal of plaque deposits from arterisclerotic arteries.)
• 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)
• Cardiovascular Surgical Instrument (FDA Code: DWS / 870.4500)
Cardiovascular surgical instruments are surgical instruments that have special features for use in cardiovascular surgery. These devices include, e.g., forceps, retractors, and scissors.
• Catheter Accessories (FDA Code: KGZ / 878.4200)
An introduction/drainage catheter is a device that is a flexible single or multilumen tube intended to be used to introduce nondrug fluids into body cavities other than blood vessels, drain fluids from body cavities, or evaluate certain physiologic conditions. Examples include irrigation and drainage catheters, pediatric catheters, peritoneal catheters (including dialysis), and other general surgical catheters. An introduction/drainage catheter accessory is intended to aid in the manipulation of or insertion of the device into the body. Examples of accessories include adaptors, connectors, and catheter needles.
• Catheter Dilator (FDA Code: GCC / 878.4200)
• Catheter Introducers (FDA Code: DYB / 870.1340)
A catheter introducer is a sheath used to facilitate placing a catheter through the skin into a vein or artery.
• Catheter Introducers, MULLINS
• Catheter Introducers, Mullins Design
• Cholangiography Catheters (FDA Code: GBZ / 878.4200)
• Constrained Elbow Prosthesis (FDA Code: JDC / 888.3150)
An elbow joint metal/polymer constrained cemented prosthesis is a device intended to be implanted to replace an elbow joint. It is made of alloys, such as cobalt-chromium-molybdenum, or of these alloys and of an ultra-high molecular weight polyethylene bushing. The device prevents dislocation in more than one anatomic plane and consists of two components that are linked together. This generic type of device is limited to those prostheses intended for use with bone cement (888.3027).
• Denis Brown Splint (FDA Code: ITN / 890.3675)
A Denis Brown splint is a device intended for medical purposes to immobilize the foot. It is used on young children with tibial torsion (excessive rotation of the lower leg) or club foot.
• Diagnostic Biliary Catheter (FDA Code: FGE / 876.5010)
A biliary catheter and accessories is a tubular flexible device used for temporary or prolonged drainage of the biliary tract, for splinting of the bile duct during healing, or for preventing stricture of the bile duct. This generic type of device may include a bile collecting bag that is attached to the biliary catheter by a connector and fastened to the patient with a strap.
• Diagnostic Intravascular Catheter (FDA Code: DQO / 870.1200)
An intravascular diagnostic catheter is a device used to record intracardiac pressures, to sample blood, and to introduce substances into the heart and vessels. Included in this generic device are right-heart catheters, left-heart catheters, and angiographic catheters, among others.
• Disposable Aspiration and Injection Needle (FDA Code: GAA / 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.
• 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.
• Disposable Surgical Instrument Kit (FDA Code: KDD / 878.4800)
• Electrocardiograph Electrode (FDA Code: DRX / 870.2360)
An electrocardiograph electrode is the electrical conductor which is applied to the surface of the body to transmit the electrical signal at the body surface to a processor that produces an electrocardiogram or vectorcardiogram.
• Electrode Recording Catheter (FDA Code: DRF / 870.1220)
An electrode recording catheter or an electrode recording probe is a device used to detect an intracardiac electrocardiogram, or to detect cardiac output or left-to-right heart shunts. The device may be unipolar or multipolar for electrocardiogram detection, or may be a platinum-tipped catheter which senses the presence of a special indicator for cardiac output or left-to-right heart shunt determinations.
• Electrosurgical Cutting and Coagulation Device (FDA Code: GEI / 878.4400)
An electrosurgical cutting and coagulation device and accessories is a device intended to remove tissue and control bleeding by use of high-frequency electrical current.
• Embolectomy Catheters (FDA Code: DXE / 870.5150)
An embolectomy catheter is a balloon-tipped catheter that is used to remove thromboemboli, i.e., blood clots which have migrated in blood vessels from one site in the vascular tree to another.
• Endoscopic Surgical Light (FDA Code: FSW / 878.4580)
A surgical lamp (including a fixture) is a device intended to be used to provide visible illumination of the surgical field or the patient.
• Extravascular Blood Flow Probe (FDA Code: DPT / 870.2120)
An extravascular blood flow probe is an extravascular ultrasonic or electromagnetic probe used in conjunction with a blood flowmeter to measure blood flow in a chamber or vessel.
• Flow Directed Catheter (FDA Code: DYG / 870.1240)
A flow-directed catheter is a device that incorporates a gas-filled balloon to help direct the catheter to the desired position.
• Foley Catheter Introducer
• General & Plastic Surgery Laparoscope (FDA Code: GCJ / 876.1500)
An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals. The device consists of various rigid or flexible instruments that are inserted into body spaces and may include an optical system for conveying an image to the user's eye and their accessories may assist in gaining access or increase the versatility and augment the capabilities of the devices. Examples of devices that are within this generic type of device include cleaning accessories for endoscopes, photographic accessories for endoscopes, nonpowered anoscopes, binolcular attachments for endoscopes, pocket battery boxes, flexible or rigid choledochoscopes, colonoscopes, diagnostic cystoscopes, cystourethroscopes, enteroscopes, esophagogastroduodenoscopes, rigid esophagoscopes, fiberoptic illuminators for endoscopes, incandescent endoscope lamps, biliary pancreatoscopes, proctoscopes, resectoscopes, nephroscopes, sigmoidoscopes, ureteroscopes, urethroscopes, endomagnetic retrievers, cytology brushes for endoscopes, and lubricating jelly for transurethral surgical instruments. This section does not apply to endoscopes that have specialized uses in other medical specialty areas and that are covered by classification regulations in other parts of the device classification regulations.
• General & Plastic Surgery Surgical Cannula (FDA Code: GEA / 878.4800)
• General & Plastic Surgery Surgical Hook (FDA Code: GDG / 878.4800)
• General Surgical Manual Instrument (FDA Code: MDM / 878.4800)
• General Surgical Scissors (FDA Code: LRW / 878.4800)
• Guidewire Catheter (FDA Code: DQX / 870.1330)
A catheter guide wire is a coiled wire that is designed to fit inside a percutaneous catheter for the purpose of directing the catheter through a blood vessel.
• Heart Stabilizer (FDA Code: MWS / 870.4500)
• Hemodialysis Catheter Repair Kit (FDA Code: NFK / 876.5540)
A blood access device and accessories is a device intended to provide access to a patient's blood for hemodialysis or other chronic uses. When used in hemodialysis, it is part of an artificial kidney system for the treatment of patients with renal failure or toxemic conditions and provides access to a patient's blood for hemodialysis. The device includes implanted blood access devices, nonimplanted blood access devices, and accessories for both the implanted and nonimplanted blood access devices.
• Implantable Clip (FDA Code: FZP / 878.4300)
An implantable clip is a clip-like device intended to connect internal tissues to aid healing. It is not absorbable.
• Implantable Staple (FDA Code: GDW / 878.4750)
An implantable staple is a staple-like device intended to connect internal tissues to aid healing. It is not absorbable.
• Implantable Venous Access Catheter Introducer Kits
• Implanted Hemodialysis Catheter (FDA Code: MSD / 876.5540)
• Implanted Subcutaneous Intravascular Port & Catheter (FDA Code: LJT / 880.5965)
A subcutaneous, implanted, intravascular infusion port and catheter is a device that consists of a subcutaneous, implanted reservoir that connects to a long-term intravascular catheter. The device allows for repeated access to the vascular system for the infusion of fluids and medications and the sampling of blood. The device consists of a portal body with a resealable septum and outlet made of metal, plastic, or combination of these materials and a long-term intravascular catheter is either preattached to the port or attached to the port at the time of device placement. The device is available in various profiles and sizes and can be of a single or multiple lumen design.
• Infusion Line Filter (FDA Code: FPB / 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.
• Intra-Aortic Balloon System (FDA Code: DSP / 870.3535)
A intra-aortic balloon and control system is a device that consists of an inflatable balloon, which is placed in the aorta to improve cardiovascular functioning during certain life-threatening emergencies, and a control system for regulating the inflation and deflation of the balloon. The control system, which monitors and is synchronized with the electrocardiogram, provides a means for setting the inflation and deflation of the balloon with the cardiac cycle.
• Intravenous Administration Kit (FDA Code: FPA / 880.5440)
• Intravenous Blood Flowmeter (FDA Code: DPW / 870.2100)
A cardiovascular blood flowmeter is a device that is connected to a flow transducer that energizes the transducer and processes and displays the blood flow signal.
• Irrigation Catheter (FDA Code: GBX / 878.4200)
• Needle Electrode (FDA Code: GXZ / 882.1350)
A needle electrode is a device which is placed subcutaneously to stimulate or to record electrical signals.
• Non-Disposable Suprapubic Trocar and Cannula (FDA Code: FBM / 876.5090)
A suprapubic urological catheter and accessories is a flexible tubular device that is inserted through the abdominal wall into the urinary bladder with the aid of a trocar and cannula. The device is used to pass fluids to and from the urinary tract. This generic type of device includes the suprapubic catheter and tube, Malecot catheter, catheter punch instrument, suprapubic drainage tube, and the suprapubic cannula and trocar.
• Non-Implanted Hemodialysis Catheters (FDA Code: MPB / 876.5540)
• One-Piece Scalpel (FDA Code: GDX / 878.4800)

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