Moeller Medical Gmbh

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Contact: Grant Geckeler
Web: http://www.moeller-medical.com
E-Mail:
Address: Wasserkuppenstrabe 29-31, Fulda 36043, Germany
Phone: +49-(661)-941-950 | Fax: +49-(661)-941-9590 | Map/Directions >>

Profile: Moeller Medical Gmbh deals with neurosurgical spine, aesthetic medicine and blood transfusion segments. Our neurosurgical product Liquoguard ® is a constant monitor of the normal CSF pressure pulsation and helps to detect catheter occlusion. This system can be connected by Luer-Lock connector to most commercially available lumbar and ventricular drainage catheters. We provide aesthetics product Vibrasat ® power, a vibration hand piece for liposuction treatments. Our tumescence local anaesthesia procedure is an anesthetic diluted within a salt solution, which is pumped directly into the patient's tissue. This method has principal advantages with any treatment that requires local anaesthesia, such as liposuction or many applications of vascular surgery. Liposat ® power is the combination of an infiltration pump, developed for tumescence local anaesthesia, with the powerful suction unit Vacusat ® power. We also develop Docon ® that monitors the blood donation process with the possibilities of modern data collection and data transmission.

FDA Registration Number: 3006611221
US Agent: N/a / N/a

13 Products/Services (Click for related suppliers)

• Blood Mixing and Weighing Device (FDA Code: KSQ / 864.9195)

A blood mixing device is a device intended for medical purposes that is used to mix blood or blood components by agitation. A blood weighing device is a device intended for medical purposes that is used to weigh blood or blood components as they are collected.

• Cement Dispenser (FDA Code: KIH / 888.4200)

A cement dispenser is a nonpowered syringe-like device intended for use in placing bone cement (888.3027) into surgical sites.

• Cohesive Seal

• CSF Drainage System

• Disposable Liposuction Cannula

• Drill Bit (FDA Code: HTW / 888.4540)

An orthopedic manual surgical instrument is a nonpowered hand-held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery. This generic type of device includes the cerclage applier, awl, bender, drill brace, broach, burr, corkscrew, countersink, pin crimper, wire cutter, prosthesis driver, extractor, file, fork, needle holder, impactor, bending or contouring instrument, compression instrument, passer, socket positioner, probe, femoral neck punch, socket pusher, reamer, rongeur, scissors, screwdriver, bone skid, staple driver, bone screw starter, surgical stripper, tamp, bone tap, trephine, wire twister, and wrench.

• Infiltration Pump, Digital Preset Monitor

• Instrument for Spine Surgery

• Instrument Surgical Guide (FDA Code: FZX / 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.

• Lipoplasty Suction System (FDA Code: MUU / 878.5040)

A suction lipoplasty system is a device intended for aesthetic body contouring. The device consists of a powered suction pump (containing a microbial filter on the exhaust and a microbial in-line filter in the connecting tubing between the collection bottle and the safety trap), collection bottle, cannula, and connecting tube. The microbial filters, tubing, collection bottle, and cannula must be capable of being changed between patients. The powered suction pump has a motor with a minimum of 1/3 horsepower, a variable vacuum range from 0 to 29.9 inches of mercury, vacuum control valves to regulate the vacuum with accompanying vacuum gauges, a single or double rotary vane (with or without oil), a single or double diaphragm, a single or double piston, and a safety trap.

• Percutaneous Biopsy Device (FDA Code: MJG / 878.4800)

• Pressure Measurement System

• Tamps (FDA Code: HXG / 888.4540)