Profile: DMC Medical Ltd. offers manufacturing, consultancy and distribution service to the medical device sector. Our product list comprises of saphenous vein distention systems, cardiac insulation pads, vein irrigation cannulas, and polycarbonate connectors. The saphenous vein distention system (SVDS) prevents overdistention of the saphenous vein during removal which can result in endothelial damage and complications such as thrombosis of the graft, occlusive subendothelial hyperplasia, accelerated graft atherosclerosis or a combination of these complications. Its features include pressure limiting balloon reservoir, 60cc syringe, one-way stopcock, irrigation cannula x 2, and sterile vein storage tray. The cardiac insulation pad is used during coronary artery bypass. It isolates the myocardium from the warmer descending thoracic aorta, liver & surrounding pericardial tissues.
The company is ISO 13485: 2003, CE certified.
FDA Registration Number: 9616679
US Agent: Charmaine Henderson / Ch Regulatory & Clinical Consultant Llc
Phone: +1-(925)-212-5264 E-Mail:
7 Products/Services (Click for related suppliers)
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• Cardiopulmonary Bypass Vascular Catheter (FDA Code: DWF / 870.4210) A cardiopulmonary bypass vascular catheter, cannula, or tubing is a device used in cardiopulmonary surgery to cannulate the vessels, perfuse the coronary arteries, and to interconnect the catheters and cannulas with an oxygenator. The device includes accessory bypass equipment. |
• Heart Stabilizer (FDA Code: MWS / 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. |
• Hydrogel Wound Dressing (W/Out Drug And/Or Biologic) (FDA Code: NAE / 878.4022) A hydrogel wound dressing is a sterile or non-sterile device intended to cover a wound, to absorb wound exudate, to control bleeding or fluid loss, and to protect against abrasion, friction, desiccation, and contamination. It consists of a nonresorbable matrix made of hydrophilic polymers or other material in combination with water (at least 50 percent) and capable of absorbing exudate. This classification does not include a hydrogel wound dressing that contains added drugs such as antimicrobial agents, added biologics such as growth factors, or is composed of materials derived from animal sources. |
• Irrigation Catheter (FDA Code: GBX / 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. |
• Medical Absorbent Fiber (FDA Code: FRL / 880.5300) A medical absorbent fiber is a device intended for medical purposes that is made from cotton or synthetic fiber in the shape of a ball or a pad and that is used for applying medication to, or absorbing small amounts of body fluids from, a patient's body surface. Absorbent fibers intended solely for cosmetic purposes are not included in this generic device category. |
• Surgical Vessel Dilator (FDA Code: DWP / 870.4475) A surgical vessel dilator is a device used to enlarge or calibrate a vessel. |
• Y Piece Breathing Circuit (FDA Code: CAI / 868.5240) An anesthesia breathing circuit is a device that is intended to administer medical gases to a patient during anesthesia. It provides both an inhalation and exhalation route and may include a connector, adaptor, and Y-piece. |