KINeSYS SPF30 Fragrance-Free Spray Австралія - англійська - Department of Health (Therapeutic Goods Administration)

kinesys spf30 fragrance-free spray

treadley pty ltd - butyl methoxydibenzoylmethane,octocrylene,octyl methoxycinnamate,octyl salicylate -

KINeSYS SPF30 Vanilla Green Tea Spray Австралія - англійська - Department of Health (Therapeutic Goods Administration)

kinesys spf30 vanilla green tea spray

treadley pty ltd - butyl methoxydibenzoylmethane,octocrylene,octyl methoxycinnamate,octyl salicylate -

KINeSYS SPF30 Clear Zinc Австралія - англійська - Department of Health (Therapeutic Goods Administration)

kinesys spf30 clear zinc

treadley pty ltd - zinc oxide, quantity: 250 mg/g - cream - excipient ingredients: dl-alpha-tocopheryl acetate; caprylic/capric/stearic triglyceride; isostearic acid; white beeswax; liquid paraffin; polyhydroxystearic acid; helianthus annuus; bisabolol; rosmarinus officinalis; mentha x piperita; cocos nucifera; soya oil; aloe vera - spf 30 broad spectrum high protection sunscreen

KINeSYS SPF30 Mango Spray Австралія - англійська - Department of Health (Therapeutic Goods Administration)

kinesys spf30 mango spray

treadley pty ltd - butyl methoxydibenzoylmethane,octocrylene,octyl methoxycinnamate,octyl salicylate -

GENESIS EQUINE ROUNDWORM TAPEWORM AND BOT TREATMENT FOR HORSES Австралія - англійська - APVMA (Australian Pesticides and Veterinary Medicines Authority)

genesis equine roundworm tapeworm and bot treatment for horses

boehringer ingelheim animal health australia pty. ltd. - ivermectin; praziquantel - oral paste - ivermectin anthelmintic active 8.0 mg/g; praziquantel anthelmintic active 100.0 mg/g - parasiticides - horse | colt | donkey | endurance horse | filly | foal | gelding | high performance horses | horses at stud | mare | pacer | pol - ascarid - parasacris equorium | bots - gasterophilus spp. | cutaneous onchocerciasis | hair worm | intestinal threadworm - s. westeri | large mouth stomach worm | large strongyles - strongylus edentatus | large strongyles - strongylus equinus | large strongyles - strongylus vulgaris | large strongyles - triodontophorus spp. | lungworm - dictyocaulus arnfieldi | neck threadworm | pinworm - oxyuris equi | small strongyles - cyathostomum spp. | small strongyles - cylicocyclus spp. | small strongyles - cylicodontophorus spp | small strongyles - cylicostephanus spp. | small strongyles - gyalocephalus spp. | summer sores | tapeworm - anoplocephala magna | tapeworm - anoplocephala perfoliata | tapeworm - paranoplocephala mammillana | bloodworm | bot fly | bot fly - oral and gastric sta | capillaria worm | cutaneous larvae | cutaneous onchocerciasis | gasterophilus haemorrhoidalis | gasterophilus inermis | gasterophilus intestinalis | gasterophilus nasalis | gasterophilus pecorum | red worm | stomach bot | summer sor

Genesis II Constrained Articular Insert - Prosthesis, knee, internal, insert component Австралія - англійська - Department of Health (Therapeutic Goods Administration)

genesis ii constrained articular insert - prosthesis, knee, internal, insert component

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.

Genesis II Cruciate Retaining Articular Insert - Prosthesis, knee, internal, insert component Австралія - англійська - Department of Health (Therapeutic Goods Administration)

genesis ii cruciate retaining articular insert - prosthesis, knee, internal, insert component

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.

Genesis II Cruciate Retaining Deep Flexion Insert - Prosthesis, knee, internal, insert component Австралія - англійська - Department of Health (Therapeutic Goods Administration)

genesis ii cruciate retaining deep flexion insert - prosthesis, knee, internal, insert component

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.

Genesis II Cruciate Retaining Femoral Component - Uncoated knee femur prosthesis Австралія - англійська - Department of Health (Therapeutic Goods Administration)

genesis ii cruciate retaining femoral component - uncoated knee femur prosthesis

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.

Genesis II Dished Articular Insert - Prosthesis, knee, internal, insert component Австралія - англійська - Department of Health (Therapeutic Goods Administration)

genesis ii dished articular insert - prosthesis, knee, internal, insert component

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.