Singapore - English - HSA (Health Sciences Authority)

zeus medical pte ltd - anaesthesiology - endotracheal tubes used in anaesthesia, emergency medicine and intensive care for airway management

Singapore - English - HSA (Health Sciences Authority)

zeus medical pte ltd - anaesthesiology - endotracheal tubes used in anaesthesia, emergency medicine and intensive care for airway management

Singapore - English - HSA (Health Sciences Authority)

zeus medical pte ltd - anaesthesiology - endotracheal tubes used in anaesthesia, emergency medicine and intensive care for airway management

Singapore - English - HSA (Health Sciences Authority)

zeus medical pte ltd - anaesthesiology - endotracheal tubes used in anaesthesia, emergency medicine and intensive care for airway management

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

smith & nephew pty ltd - 46585 - prosthesis, knee, internal, insert component - an implantable device designed to articulate with the femoral component of a knee joint prosthesis during primary knee joint replacement. it is a one-piece contoured ultra-high molecular weight polyethylene (uhmwpe) insert which locks into a cemented tibial tray. 1. rheumatoid arthritis. 2. post-traumatic arthritis, osteoarthritis, or degenerative arthritis. 3. failed, unicompartmental replacement, or total knee replacement. 4. posterior stabilized knee systems are designed for use in patients in primary and revision surgery, where the anterior and posterior cruciate ligaments are incompetent and the collateral ligaments remain intact. 5. constrained knee systems are designed for use in patients in primary and revision surgery, where the posterior cruciate ligament and one or both of the collateral ligaments (i.e. medial collateral and/or lateral collateral ligament) are incompetent.

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

smith & nephew pty ltd - 46585 - prosthesis, knee, internal, insert component - an implantable device designed to articulate with the femoral component of a knee joint prosthesis during primary knee joint replacement. it is a one-piece contoured ultra-high molecular weight polyethylene (uhmwpe) insert which locks into the tibial tray. 1. rheumatoid arthritis. 2. post-traumatic arthritis, osteoarthritis, or degenerative arthritis. 3. failed, unicompartmental replacement, or total knee replacement. 4. posterior stabilized knee systems are designed for use in patients in primary and revision surgery, where the anterior and posterior cruciate ligaments are incompetent and the collateral ligaments remain intact. 5. constrained knee systems are designed for use in patients in primary and revision surgery, where the posterior cruciate ligament and one or both of the collateral ligaments (i.e. medial collateral and/or lateral collateral ligament) are incompetent.

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

smith & nephew pty ltd - 46585 - prosthesis, knee, internal, insert component - an implantable device designed to articulate with the femoral component of a knee joint prosthesis during primary knee joint replacement. it is a one-piece contoured ultra-high molecular weight polyethylene (uhmwpe) insert which locks into the tibial tray. 1. rheumatoid arthritis. 2. post-traumatic arthritis, osteoarthritis, or degenerative arthritis. 3. failed osteotomies, unicompartmental replacement, or total knee replacement. 4. posterior stabilized knee systems are designed for use in patients in primary and revision surgery, where the anterior and posterior cruciate ligaments are incompetent and the collateral ligaments remain intact. 5. constrained knee systems are designed for use in patients in primary and revision surgery, where the posterior cruciate ligament and one or both of the collateral ligaments (i.e. medial collateral and/or lateral collateral ligament) are incompetent.

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

smith & nephew pty ltd - 32831 - uncoated knee femur prosthesis - a sterile implantable device designed to replace the femoral condyles (femoral component) during primary replacement of the knee joint. the device is designed to articulate with tibial and, if required, patellar prosthetic components of the knee joint. following resection of the femur, the femoral component is intended to be implanted with bone cement. a cemented co-cr-mo alloy cruciate retaining femoral component. indications for use include rheumatoid arthritis; post-traumatic arthritis, osteoarthritis, or degenerative arthritis; failed osteotomies, unicompartmental replacement or total knee replacement.

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

smith & nephew pty ltd - 46585 - prosthesis, knee, internal, insert component - an implantable device designed to articulate with the femoral component of a knee joint prosthesis during primary knee joint replacement. it is a one-piece contoured ultra-high molecular weight polyethylene (uhmwpe) insert which locks into the tibial tray. 1. rheumatoid arthritis. 2. post-traumatic arthritis, osteoarthritis, or degenerative arthritis. 3. failed, unicompartmental replacement, or total knee replacement. 4. posterior stabilized knee systems are designed for use in patients in primary and revision surgery, where the anterior and posterior cruciate ligaments are incompetent and the collateral ligaments remain intact. 5. constrained knee systems are designed for use in patients in primary and revision surgery, where the posterior cruciate ligament and one or both of the collateral ligaments (i.e. medial collateral and/or lateral collateral ligament) are incompetent.

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

smith & nephew pty ltd - 32832 - uncoated knee tibia prosthesis, metallic - a sterile implantable device designed to replace the tibial condyles during primary replacement of the knee joint. the tibial base acts as a tray and is designed to hold an insert which articulates with the femoral prosthetic component of the knee joint. the tibia is resected and the implantation of the tibial tray is intended to be performed with bone cement. a cemented titanium alloy tibial base component. indications for use include rheumatoid arthritis; post-traumatic arthritis, osteoarthritis, or degenerative arthritis; failed osteotomies, unicompartmental replacement or total knee replacement. posterior stabilized knee systems are designed for use in patients in primary and revision surgery, where the anterior and posterior cruciate ligaments are incompetent and the collateral ligaments remain intact. constrained knee systems are designed for use in patients in primary and revision surgery, where the posterior cruciate ligament and one or both of the collateral ligaments (i.e. medial collateral and/or lateral collateral ligament) are incompetent.