Benchmark Electronics (Thailand) Public Company Ltd

Contact: Greg Ruben
Address: 94 Moo 1, Hi-Tech Ind. Estate, Banlane, Bang-Pa-In, Ayudhaya 13160, Thailand | Map/Directions >>

Profile: Benchmark Electronics (Thailand) Public Company Ltd offers anesthetic infusion pumps, blood collection lancets and implantable electrical stimulators.

FDA Registration Number: 3003899230
US Agent: Greg S Ruben / Benchmark Electronics, Inc.
Phone: +1-(507)-453-4891 Fax: +1-(507)-453-4700 E-Mail:

25 Products/Services (Click for related suppliers)

• Anesthetic Infusion Pump (FDA Code: FRN / 880.5725)

An infusion pump is a device used in a health care facility to pump fluids into a patient in a controlled manner. The device may use a piston pump, a roller pump, or a peristaltic pump and may be powered electrically or mechanically. The device may also operate using a constant force to propel the fluid through a narrow tube which determines the flow rate. The device may include means to detect a fault condition, such as air in, or blockage of, the infusion line and to activate an alarm.

• Assayed and Unassayed Single (Specified) Analyte Controls (FDA Code: JJX / 862.1660)

A quality control material (assayed and unassayed) for clinical chemistry is a device intended for medical purposes for use in a test system to estimate test precision and to detect systematic analytical deviations that may arise from reagent or analytical instrument variation. A quality control material (assayed and unassayed) may be used for proficiency testing in interlaboratory surveys. This generic type of device includes controls (assayed and unassayed) for blood gases, electrolytes, enzymes, multianalytes (all kinds), single (specified) analytes, or urinalysis controls.

• Automatic Implantable Cardioverter Defibrillator With Cardiac Resynchronization (FDA Code: NIK)

• Automatic Implantable Cardioverter-defibrillator (FDA Code: LWS)

• Blood Collection Lancet (FDA Code: FMK / 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.

• Discrete Photometric Chemistry Analyzer (FDA Code: JJE / 862.2160)

A discrete photometric chemistry analyzer for clinical use is a device intended to duplicate manual analytical procedures by performing automatically various steps such as pipetting, preparing filtrates, heating, and measuring color intensity. This device is intended for use in conjunction with certain materials to measure a variety of analytes. Different models of the device incorporate various instrumentation such as micro analysis apparatus, double beam, single, or dual channel photometers, and bichromatic 2-wavelength photometers. Some models of the device may include reagent-containing components that may also serve as reaction units.

• Dual Chamber Implantable Pulse-Generator (FDA Code: LWP)

• Electrocardiograph (FDA Code: DPS / 870.2340)

An electrocardiograph is a device used to process the electrical signal transmitted through two or more electrocardiograph electrodes and to produce a visual display of the electrical signal produced by the heart.

• Electrocardiograph Transmitter/Receiver System (FDA Code: DXH / 870.2920)

A telephone electrocardiograph transmitter and receiver is a device used to condition an electrocardiograph signal so that it can be transmitted via a telephone line to another location. This device also includes a receiver that reconditions the received signal into its original format so that it can be displayed. The device includes devices used to transmit and receive pacemaker signals.

• External Pacemaker Pulse Generator (FDA Code: DTE / 870.3600)

An external pacemaker pulse generator is a device that has a power supply and electronic circuits that produce a periodic electrical pulse to stimulate the heart. This device, which is used outside the body, is used as a temporary substitute for the heart's intrinsic pacing sytem until a permanent pacemaker can be implanted, or to control irregular heartbeats in patients following cardiac surgery or a myocardial infarction. The device may have adjustments for impulse strength, duration, R-wave sensitivity, and other pacing variables.

• Glucose Glucose Dehydrogenase (FDA Code: LFR / 862.1345)

A glucose test system is a device intended to measure glucose quantitatively in blood and other body fluids. Glucose measurements are used in the diagnosis and treatment of carbohydrate metabolism disorders including diabetes mellitus, neonatal hypoglycemia, and idiopathic hypoglycemia, and of pancreatic islet cell carcinoma.

• Glucose Oxidase, Glucose (FDA Code: CGA / 862.1345)

• Hydroxybutyric Dehydroge Dinitrophenyl Hydrazone Measurement (Colorimetric) (FDA Code: JKF / 862.1380)

A hydroxybutyric dehydrogenase test system is a device intended to measure the activity of the enzyme alpha-hydroxybutric dehydrogenase (HBD) in plasma or serum. HBD measurements are used in the diagnosis and treatment of myocardial infarction, renal damage (such as rejection of transplants), certain hematological diseases (such as acute leukemias and megaloblastic anemias) and, to a lesser degree, liver disease.

• Implantable Electrical Stimulator (FDA Code: EZW / 876.5270)

An implanted electrical urinary device is a device intended for treatment of urinary incontinence that consists of a receiver implanted in the abdomen with electrodes for pulsed-stimulation that are implanted either in the bladder wall or in the pelvic floor, and a battery-powered transmitter outside the body.

• Implantable Permanent Pulse Generator (FDA Code: NVZ)

• Implanted Electrical Stimulator (FDA Code: MHY)

• Implanted Electrical Stimulator For Parkinsonian Symptoms (FDA Code: NHL)

• Implanted Programmable Infusion Pump (FDA Code: LKK)

• Implanted Subcortical Electrical Stimulator (Motor Disorders) (FDA Code: MRU)

• Indirect Pacemaker Generator Function Analyzer (FDA Code: KRE / 870.3640)

An indirect pacemaker generator function analyzer is an electrically powered device that is used to determine pacemaker function or pacemaker battery function by periodically monitoring an implanted pacemaker's pulse rate and pulse width. The device is noninvasive, and it detects pacemaker pulse rate and width via external electrodes in contact with the patient's skin.

• Over-The-Counter Blood Glucose Test System (FDA Code: NBW / 862.1345)

• Pacemaker Programmer (FDA Code: KRG / 870.3700)

A pacemaker programmer is a device used to change noninvasively one or more of the electrical operating characteristics of a pacemaker.

• Peristaltic Infusion Pump (FDA Code: FRN / 880.5725)

• Programmable Implantable Heart Pacemaker (FDA Code: DXY / 870.3610)

An implantable pacemaker pulse generator is a device that has a power supply and electronic circuits that produce a periodic electrical pulse to stimulate the heart. This device is used as a substitute for the heart's intrinsic pacing system to correct both intermittent and continuous cardiac rhythm disorders. This device includes triggered, inhibited, and asynchronous devices implanted in the human body.

• Totally Implanted Spinal Cord Stimulator for Pain Relief (FDA Code: LGW)