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 Incandescent Surgical Lamp Suppliers > Advanced Surgical Design And Manufacture Limited.

Advanced Surgical Design And Manufacture Limited.


Contact: James Logan
Web: http://www.asdm.com.au
Address: 2/12 Frederick St., St.Leonards, New South Wales 2065, Australia
Phone: +61-(2)-9439 4448 | Fax: +61-(2)-9439 4441 | Map/Directions >>
 
 

Profile: Advanced Surgical Design & Manufacture Limited manufacturers medical devices including prosthetic implants and surgical tools. Our product area includes orthopedic, vascular and medical devices. Our orthopedic product provides active total knee replacement. Our titan surgical-grade titanium custom cranio-facial implant system enables surgeons to replace missing or defective pieces of skull or facial bone with a stable substitute that has been contoured to exactly replicate the missing piece. Titan implants are secured with surgical-grade titanium self-tapping bone screws fixed by sterile screwdriver blades driven by sterile twist drills. The titan system also includes a range of titanium screws and plates for trauma and reconstructive surgery.

16 Products/Services (Click for related suppliers)  
• Arthroscopic Accessories (FDA Code: NBH / 888.1100)
An arthroscope is an electrically powered endoscope intended to make visible the interior of a joint. The arthroscope and accessories also is intended to perform surgery within a joint.
• Audiometers (FDA Code: EWO / 874.1050)
An audiometer or automated audiometer is an electroacoustic device that produces controlled levels of test tones and signals intended for use in conducting diagnostic hearing evaluations and assisting in the diagnosis of possible otologic disorders.
• Broach (FDA Code: HTQ / 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.
• Depth Gauge (FDA Code: HTJ / 888.4300)
A depth gauge for clinical use is a measuring device intended for various medical purposes, such as to determine the proper length of screws for fastening the ends of a fractured bone.
• Drill Bit (FDA Code: HTW / 888.4540)
• Flexible Depth Gauge (FDA Code: HTJ / 888.4300)
• Impactor (FDA Code: HWA / 888.4540)
• 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.
• Orthopedic Manual Surgical Instrument (FDA Code: LXH / 888.4540)
• Screwdriver (FDA Code: HXX / 888.4540)
• Semi-Constrained Femorotibial Knee Prosthesis (FDA Code: HRY / 888.3530)
A knee joint femorotibial metal/polymer semi-constrained cemented prosthesis is a device intended to be implanted to replace part of a knee joint. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across-the-joint. This generic type of device includes prostheses that consist of a femoral component made of alloys, such as cobalt-chromium-molybdenum, and a tibial component made of ultra-high molecular weight polyethylene and is limited to those prostheses intended for use with bone cement (888.3027).
• Semi-Constrained Patellofemorotibial Knee Prosthesis (FDA Code: JWH / 888.3560)
A knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis is a device intended to be implanted to replace a knee joint. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across-the-joint. This generic type of device includes prostheses that have a femoral component made of alloys, such as cobalt-chromium-molybdenum, and a tibial component or components and a retropatellar resurfacing component made of ultra-high molecular weight polyethylene. This generic type of device is limited to those prostheses intended for use with bone cement (888.3027).
• Small Depth Gauge (FDA Code: HTJ / 888.4300)
• Surgical Trays (FDA Code: LRP / 878.4800)
• Surgical Trays (FDA Code: LRP / 878.4800)
• Templates (FDA Code: HWT / 888.4800)
A template for clinical use is a device that consists of a pattern or guide intended for medical purposes, such as selecting or positioning orthopedic implants or guiding the marking of tissue before cutting.

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