United States - English - NLM (National Library of Medicine)

newton laboratories, inc. - lycopus virginicus (unii: twh5125q6f) (lycopus virginicus - unii:twh5125q6f), anemone pulsatilla (unii: i76kb35jev) (anemone pulsatilla - unii:i76kb35jev), vipera berus venom (unii: 0oro6nca4m) (vipera berus venom - unii:0oro6nca4m), echinacea, unspecified (unii: 4n9p6cc1dx) (echinacea, unspecified - unii:4n9p6cc1dx), hypericum perforatum (unii: xk4iux8mnb) (hypericum perforatum - unii:xk4iux8mnb), aconitum napellus (unii: u0nq8555jd) (aconitum napellus - unii:u0nq8555jd), barium carbonate (unii: 6p66 - formulated for symptoms such as fear, cold hands & feet, headache, weakness, sallow skin and palpitations. formulated for symptoms such as fear, cold hands & feet, headache, weakness, sallow skin and palpitations.

Australia - English - Department of Health (Therapeutic Goods Administration)

link orthopaedics australia pty ltd - 33178 - revision uncoated hip femur prosthesis - the modular distal femoral replacement components are used to replace the distal femur and is made from cocrmo, uhmwpe and is anatomically adapted. the component can be intra-operatively flexible and used with the megasystem c system through complete compatibility. the distal femoral replacement modular component is part of the endo-model rotational knee system indicated for severe joint diseases with limitation of mobility due to degenerative, rheumatoid or post-traumatic arthrosis or arthritis. joint fractures which disallow an osteosynthetic reconstruction; bone necroses; bicondylar arthrosis by partly damaged collateral ligaments; revision surgery after hinge knee or rotational knee joint; revision surgery by insufficient / inadequate bone mass.

Australia - English - Department of Health (Therapeutic Goods Administration)

link orthopaedics australia pty ltd - 32832 - uncoated knee tibia prosthesis, metallic - the connection component has a neutral offset, is made of cocrmo, uhmwpe and is coupled together with the tibial component. the component is interchangeable between the rotational and hinge knee and is intra-operatively compatible with the megasystem c system. the connection component of the endo-model sl rotational and hinge knee system indicated for use in severe joint diseases with limitation of mobility due to degenerative, rheumatoid or post-traumatic arthrosis or arthritis. joint fractures which disallow an osteosynthetic reconstruction ? bone necroses ? bicondylar arthritis with insufficient colateral ligaments ? bicondylar arthritis with completely destructed collateral ligaments and muscular instability ? revision after primary total knee replacement ? revision surgery after hinge knee or rotational revision surgery with insufficient bone quality

Australia - English - Department of Health (Therapeutic Goods Administration)

link orthopaedics australia pty ltd - 32832 - uncoated knee tibia prosthesis, metallic - the tibial component has a neutral offset, is made of cocrmo, uhmwpe and is for cemented use. the component is interchangeable and compatible with the megasystem c system the tibial component of the endo-model sl rotational and hinge knee system indicated for use in severe joint diseases with limitation of mobility due to degenerative, rheumatoid or post-traumatic arthrosis or arthritis; joint fractures which disallow an osteosynthetic reconstruction; bone necrosis; bicondylar arthritis with insufficient collateral ligaments; revision after primary total knee replacement; revision surgery after hinge knee or rotational; revision surgery with insufficient bone quality.

Australia - English - Department of Health (Therapeutic Goods Administration)

link orthopaedics australia pty ltd - 32832 - uncoated knee tibia prosthesis, metallic - the tibial component system is modular with a neutral offset. the antiluxation effect through extension of the rotational pivot and use of antiluxation mechanism and has intraoperative flexibility through complete compatibility with the megasystem c system. the tibial component system of the endo-model sl rotational and hinge knee system indicated for use in severe joint diseases with limitation of mobility due to degenerative, rheumatoid or post-traumatic arthrosis or arthritis. joint fractures which disallow an osteosynthetic reconstruction ? bone necroses ? bicondylar arthritis with insufficient colateral ligaments ? bicondylar arthritis with completely destructed collateral ligaments and muscular instability ? revision after primary total knee replacement ? revision surgery after hinge knee or rotational revision surgery with insufficient bone quality

Australia - English - Department of Health (Therapeutic Goods Administration)

link orthopaedics australia pty ltd - 32832 - uncoated knee tibia prosthesis, metallic - the tibial component can be integrated through compatibility with the modular megasystem c and gemini sl components. it is made of tilastan and uhmwpe. the component can be coupled with the modular stem and has a neutral off set. the proximal tibial replacement is a component of the endo-model sl rotational and hinge knee system indicated for use in severe joint diseases with limitation of mobility due to degenerative, rheumatoid or post-traumatic arthrosis or arthritis; joint fractures which disallow an osteosynthetic reconstruction; bone necroses; bicondylar arthritis with insufficient collateral ligaments; revision after primary total knee replacement; revision surgery after hinge knee or rotational; revision surgery with insufficient bone quality.

Australia - English - Department of Health (Therapeutic Goods Administration)

link orthopaedics australia pty ltd - 33666 - uncoated knee tibia/insert prosthesis - cocrmo alloy tibial component integrated through compatibility with the modular megasystem c and sl components. pointed stem locking screw located inside taper of each joint component. inside packing unit of each joint component includes counter screw (+ replacement screw) to secure stem locking screw. prosthesis is broadly supported on respective knee joint surfaces so compression strength of cancellous bone in the tibia, is not exceeded. tibia is coupled with the femur having neutral off set. the tibial component of the endo-model rotational and hinge knee system and is indicated for use in severe joint diseases with limitation of mobility due to degenerative, rheumatoid or post-traumatic arthrosis or arthritis; joint fractures which disallow an osteosynthetic reconstruction; bone necrose; bicondylar arthrosis by partly damaged collateral ligaments; revision after primary knee replacement; revision surgery after hinge knee or rotational knee joint; revision surgery by insufficient / inadequate bone mass.

Australia - English - Department of Health (Therapeutic Goods Administration)

link orthopaedics australia pty ltd - 32831 - uncoated knee femur prosthesis - the femoral rotational component is made from cocrmo alloy, and is used with cement. the femoral prosthesis has a normal valgus position of 6? and is broadly supported on the respective knee joint surfaces so that the compression strength of the cancellous bone in the femur, is not exceeded. the flanges of the femoral component are anatomically shaped. its ventral depression provides a smooth transition from the implant to the trochlear groove the femoral joint component of the endo-model ? m modular intracondylar total knee joint prosthesis which is an additional version of the endo-model rotational and hinge knee system, indicated for use in severe joint diseases with limitation of mobility due to degenerative, rheumatoid or post-traumatic arthrosis or arthritis; joint fractures which disallow an osteosynthetic reconstruction; bone necrose; bicondylar arthrosis by partly damaged collateral ligaments; revision surgery after hinge knee or rotational knee joint; revision surgery by insufficient / inadequte bone mass

United States - English - NLM (National Library of Medicine)

smiths medical asd, inc. - chlorhexidine gluconate (unii: mor84mud8e) (chlorhexidine - unii:r4ko0dy52l), isopropyl alcohol (unii: nd2m416302) (isopropyl alcohol - unii:nd2m416302) - chlorhexidine gluconate 20 mg in 1 ml - antiseptic for the preparation of the patient's skin prior to surgery. helps to reduce bacteria that potentially can cause skin infection. use with care in premature infants or infants under 2 months of age. these products may cause irritation or chemical burns.use in a well ventilated areamaximal treatment area for one applicator is approximately 4 in. x 5 in. (130 cm 2)remove applicator from package; do not touch spongehold the applicator with the sponge down. pinch wings only once to activate the ampule and release the antiseptic.wet the sponge by pressing and releasing the sponge against the treatment area until liquid is visible on the skincompletely wet the treatment area with antisepticdry surgical sites (e.g., abdomen or arm): use gentle repeated back-and-forth strokes for 30 secondsmoist surgical sites (e.g., inguinal fold): use gentle repeated back-and-forth strokes for 2 minutesallow the solution to completely dry (minimum of 3 minutes on hairless skin; up to 1 hour in hair). do not blot or wipe aw

Canada - English - Health Canada

hill dermaceuticals inc - fluocinolone acetonide - emulsion - 0.01% - fluocinolone acetonide 0.01% - anti-inflammatory agents