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Owen Mumford Inc.

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Web: http://www.owenmumford.com
E-Mail:
Address: 1755-A West Oak Commons Court, Marietta, Georgia 30062, USA
Phone: +001-(800)-421-6936 | Fax: +001-(770)-977-2866 | Map/Directions >>
 
 

Profile: Owen Mumford Inc. designs and produces a range of medical devices & disposables, which are used by healthcare professionals & consumers worldwide. Unilet lancets renders a complete range of needle sizes to ensure that accurate blood samples for all popular meters can be obtained with any skin type. Our autodrop is specially designed to overcome the difficulties experienced by many when administering eyedrops. Our Amielle comfort vaginal dilators offer an effective way for women to take an active role in their treatment of sexual disorders such as vaginismus and dyspareunia, in the privacy and comfort of their own surroundings. Our Neurotips are sterile, single-use neurological examination pins which avoid the risk of cross-infection and skin puncture.

The company has revenues of USD 25-50 Million, has ~250 employees and is ISO 9001, CE certified.

FDA Registration Number: 8021764
US Agent: Travis Shaw / Owen Mumford Usa, Inc.
Phone: +1-(800)-421-6936  Fax: +1-(770)-977-2866  E-Mail:

34 Products/Services (Click for related suppliers)  
• Artery Blood Sampling Kits
• Blood Collect Tubes
• 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.
• Blood Collection Needles
• Blood Lancet Needle (Blade Type)
• Blood Lancet Needle (Pen Type)
• Blood Lancets
• Blood Sampling Kit
• Disposable Blood Lancet Needles
• Disposable Syringes
• Dry and Liquid Heparin Arterial Blood Sampling Kits
• ENT Dropper (FDA Code: KCM / 874.5220)
An ear, nose, and throat drug administration device is one of a group of ear, nose, and throat devices intended specifically to administer medicinal substances to treat ear, nose, and throat disorders. These instruments include the powder blower, dropper, ear wick, manual nebulizer pump, and nasal inhaler.
• Esthesiometers (FDA Code: GXB / 882.1500)
An esthesiometer is a mechanical device which usually consists of a single rod or fiber which is held in the fingers of the physician or other examiner and which is used to determine whether a patient has tactile sensitivity.
• External Penile Rigidity Device (FDA Code: LKY / 876.5020)
• Eye Dropper
• General Diagnostic Supplies
• General Medical Supplies
• General Surgical Aids
• General Surgical Instruments
• Hollow Fiber Capillary Dialyzer (FDA Code: FJI / 876.5820)
A hemodialysis system and accessories is a device that is used as an artificial kidney system for the treatment of patients with renal failure or toxemic conditions and that consists of an extracorporeal blood system, a conventional dialyzer, a dialysate delivery system, and accessories. Blood from a patient flows through the tubing of the extracorporeal blood system and accessories to the blood compartment of the dialyzer, then returns through further tubing of the extracorporeal blood system to the patient. The dialyzer has two compartments that are separated by a semipermeable membrane. While the blood is in the blood compartment, undesirable substances in the blood pass through the semipermeable membrane into the dialysate in the dialysate compartment. The dialysate delivery system controls and monitors the dialysate circulating through the dialysate compartment of the dialyzer.
• Insulin Disposable Syringes Kits
• Insulin Injector
• Insulin Syringe Needle Clipper
• Insulin Syringes
• Lancet Devices
• Medication Injector
• 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.
• Plastic Blood Lancets
• 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.
• Spirometer & Respiratory Aids
• Stainless Steel Blood Lancets
• Syringe Needle Introducer (FDA Code: KZH / 880.6920)
A syringe needle introducer is a device that uses a spring-loaded mechanism to drive a hypodermic needle into a patient to a predetermined depth below the skin surface.
• Vacuum Sample Tube with Anticoagulant (FDA Code: GIM / 862.1675)
A blood specimen collection device is a device intended for medical purposes to collect and to handle blood specimens and to separate serum from nonserum (cellular) components prior to further testing. This generic type device may include blood collection tubes, vials, systems, serum separators, blood collection trays, or vacuum sample tubes.
• Vaginal Stent (FDA Code: KXP / 884.3900)
A vaginal stent is a device used to enlarge the vagina by stretching, or to support the vagina and to hold a skin graft after reconstructive surgery.

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