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

bard australia pty ltd - 47201 - collagen haemostatic agent - avitene? (mch) is an absorbable topical hemostatic agent prepared as a dry, sterile, fibrous, water insoluble partial hydrochloric acid salt of purified bovine corium collagen. avitene? (mch) is used in surgical procedures as an adjunct to hemostasis when control of bleeding by ligature or conventional procedures is ineffective or impractical.

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

bard australia pty ltd - 47201 - collagen haemostatic agent - avitene? (mch) is an absorbable topical hemostatic agent prepared as a dry, sterile, fibrous, water insoluble partial hydrochloric acid salt of purified bovine corium collagen. avitene? (mch) is used in surgical procedures as an adjunct to hemostasis when control of bleeding by ligature or conventional procedures is ineffective or impractical.

Malaysia - English - NPRA (National Pharmaceutical Regulatory Agency, Bahagian Regulatori Farmasi Negara)

nano wellness sdn bhd - collagen peptide; collagen peptide; collagen peptide; chicken eggshell membrane; collagen -

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

viatrexx bio incorporated - collagen 8x, 200k - to help support collagen formation

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

uriel pharmacy inc. - bovine type i collagen (unii: fhj3atl51c) (bovine type i collagen - unii:fhj3atl51c) - directions: for oral use only. use: promotes healthy balance of homologous organs.

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

pacific dental specialties pty ltd - 58709 - collagen dental regeneration membrane - cytoplast? collagen membranes is a resorbable, cell-occlusive barrier membranes used in guided tissue and bone regeneration procedures in oral surgery to manage oral wounds and assist in wound healing. cytoplast is a rtm collagen membrane is a bioresorbable, implantable collagen material (cell-occlusive barrier membranes ) that is intended for used for periodontal and/or dental surgery procedures as a material for placement in the area of periodontal and/or dental surgery procedures as a material for placement in the area of periodontal defects, dental implant, bone defect or ridge construction to aid in wound healing post surgery. the multilayer construction allows tissue integration into outer layers while preventing direct passage of bacteria and epithelial cells.

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

implant direct oceania pty ltd - 58709 - collagen dental regeneration membrane - reguarde? collagen membranes is a resorbable, cell-occlusive barrier membranes used in guided tissue and bone regeneration procedures in oral surgery to manage oral wounds and assist in wound healing. "reguarde? collagen membrane is a bioresorbable, implantable collagen material (cell-occlusive barrier membranes ) that is intended for use in periodontal and/or dental surgery procedures as a material for placement in the area of periodontal and/or dental surgery procedures as a material for placement in the area of periodontal defects, dental implant, bone defect or ridge construction to aid in wound healing post surgery".

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

neoss australia pty ltd - 58709 - collagen dental regeneration membrane - the bone defect is exposed and autologous, demineralized bone or ceramic materials may be used to fill the defect. neogen collagen flex may be placed either dry or hydrated over the defect -hydration by sterile water or saline solution. the membrane can be trimmed to the size and shape - it should overlap the walls of the defect by at least 2 mm to allow complete bone contact. fixation with sutures or resorbable tacks. neogen collagen flex is resorbed in 12 to 16 weeks. neogen collagen flex is a bioresorbable, implantable collagen material that is intended for use in oral surgical procedures as a resorbable membrane material for use in ? simultaneous use of guided bone regeneration (gbr)-membrane and implants; ? augmentation around implants placed in immediate extraction sockets; ? augmentation around implants placed in delayed extraction sockets; ? localized ridge augmentation for later implantation; ? alveolar ridge reconstruction for prosthetic treatment; ? filling of bone defects after root resection, cystectomy or removal of retained teeth; ? guided bone regeneration in dehiscence defects; and ? guided tissue regeneration procedures in periodontal defects.

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

novartis pharmaceuticals corporation - tisagenlecleucel (unii: q6c9whr03o) (tisagenlecleucel - unii:q6c9whr03o) - tisagenlecleucel 2000000 - kymriah is a cd19-directed genetically modified autologous t cell immunotherapy indicated for the treatment of: patients up to 25 years of age with b-cell precursor acute lymphoblastic leukemia (all) that is refractory or in second or later relapse. adult patients with relapsed or refractory (r/r) large b-cell lymphoma after two or more lines of systemic therapy including diffuse large b-cell lymphoma (dlbcl) not otherwise specified, high grade b-cell lymphoma and dlbcl arising from follicular lymphoma. limitation of use: kymriah is not indicated for treatment of patients with primary central nervous system lymphoma. adult patients with relapsed or refractory (r/r) follicular lymphoma (fl) after two or more lines of systemic therapy. this indication is approved under accelerated approval based on response rate and duration of response [see clinical studies (14.3)] . continued approval for this indication may be contingent upon verification and description of clinical benefit in confirmatory trial(s). none. r

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

viatrexx bio incorporated - pork collagen (unii: i8442u2g7j) (pork collagen - unii:i8442u2g7j) - viatrexx-collagen  a sterile, injectable, biodegradable, clear isotonic liquid that is injected into the various layers of the skin, muscles, ligaments, joints, other body tissues or added to an iv, either as a push or into the bag. this product should not be used in patients with a known hypersensitivity to any ingredient found in the formula, porcine products, isotonic saline or benzyl alcohol, or patients with a history of severe allergies. as with all injections, epinephrine injection (1:1,000) must be immediately available should an acute anaphylactoid reaction occur due to any component of the injection. this product contains 1% benzyl alcohol. benzyl alcohol has been reported to be associated with a fatal "gasping syndrome" in premature infants. due to the benzyl alcohol content, this product should not be given to a pregnant woman. this product should not be used in patients with a known hypersensitivity to any ingredient in this formula, porcine products, isotonic saline or benzyl alcohol, or patient