AROA BIOSURGERY LIMITED

Address:2 Kingsford Smith Place,Airport Oaks Auckland,NZ

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Device Description : Endoform Surface is intended for applications in plastic and reconstructive surg Endoform Surface is intended for applications in plastic and reconstructive surgery or to cover, protect, and provide a moist wound environment. The device may be fixed, via sutures, staples, or tacks to the surrounding tissue, if desired.

Device Class : 2

Duns Number: 594540572

Premarket Exempt : No

Product Code : KGN, FTM

Prescription Use : Yes

Device Count : 1

- Catalog Number :

Device Description : Endoform Surface is intended for applications in plastic and reconstructive surg Endoform Surface is intended for applications in plastic and reconstructive surgery or to cover, protect, and provide a moist wound environment. The device may be fixed, via sutures, staples, or tacks to the surrounding tissue, if desired.

Device Class : 2

Duns Number: 594540572

Premarket Exempt : No

Product Code : FTM, KGN

Prescription Use : Yes

Device Count : 1

- Catalog Number :

Device Description : Endoform Surface is intended for applications in plastic and reconstructive surg Endoform Surface is intended for applications in plastic and reconstructive surgery or to cover, protect, and provide a moist wound environment. The device may be fixed, via sutures, staples, or tacks to the surrounding tissue, if desired.

Device Class : 2

Duns Number: 594540572

Premarket Exempt : No

Product Code : KGN, FTM

Prescription Use : Yes

Device Count : 1

- Catalog Number :

Device Description : Endoform Surface is intended for applications in plastic and reconstructive surg Endoform Surface is intended for applications in plastic and reconstructive surgery or to cover, protect, and provide a moist wound environment. The device may be fixed, via sutures, staples, or tacks to the surrounding tissue, if desired.

Device Class : 2

Duns Number: 594540572

Premarket Exempt : No

Product Code : KGN, FTM

Prescription Use : Yes

Device Count : 1

- Catalog Number : F10244-2530P

Device Description : OviTex™ Core Reinforced Tissue Matrix with Permanent Polymer (OviTex) is a steri OviTex™ Core Reinforced Tissue Matrix with Permanent Polymer (OviTex) is a sterile bioscaffold composed of ovine (sheep) derived extracellular matrix (ECM) and monofilament polypropylene colored with ([phathalocyaninato(2-)] copper). OviTex will incorporate into the recipient tissue with associated cellular and microvascular ingrowth.OviTex is provided in various shapes and sizes to suit surgeon preference and the complexity of the soft tissue repair. The device may be trimmed to a desired shape to further accommodate an individual patient’s requirements.

Device Class : 2

Duns Number: 594540572

Premarket Exempt : No

Product Code : FTM, FTL

Prescription Use : Yes

Device Count : 1

- Catalog Number : F10244-2540P

Device Description : OviTex™ Core Reinforced Tissue Matrix with Permanent Polymer (OviTex) is a steri OviTex™ Core Reinforced Tissue Matrix with Permanent Polymer (OviTex) is a sterile bioscaffold composed of ovine (sheep) derived extracellular matrix (ECM) and monofilament polypropylene colored with ([phathalocyaninato(2-)] copper). OviTex will incorporate into the recipient tissue with associated cellular and microvascular ingrowth.OviTex is provided in various shapes and sizes to suit surgeon preference and the complexity of the soft tissue repair. The device may be trimmed to a desired shape to further accommodate an individual patient’s requirements.

Device Class : 2

Duns Number: 594540572

Premarket Exempt : No

Product Code : FTL, FTM

Prescription Use : Yes

Device Count : 1

- Catalog Number : F10246-2530P

Device Description : OviTex™ Core Reinforced Tissue Matrix with Permanent Polymer (OviTex) is a steri OviTex™ Core Reinforced Tissue Matrix with Permanent Polymer (OviTex) is a sterile bioscaffold composed of ovine (sheep) derived extracellular matrix (ECM) and monofilament polypropylene colored with ([phathalocyaninato(2-)] copper). OviTex will incorporate into the recipient tissue with associated cellular and microvascular ingrowth.OviTex is provided in various shapes and sizes to suit surgeon preference and the complexity of the soft tissue repair. The device may be trimmed to a desired shape to further accommodate an individual patient’s requirements.

Device Class : 2

Duns Number: 594540572

Premarket Exempt : No

Product Code : FTL, FTM

Prescription Use : Yes

Device Count : 1

- Catalog Number : F10246-2540P

Device Description : OviTex™ Core Reinforced Tissue Matrix with Permanent Polymer (OviTex) is a steri OviTex™ Core Reinforced Tissue Matrix with Permanent Polymer (OviTex) is a sterile bioscaffold composed of ovine (sheep) derived extracellular matrix (ECM) and monofilament polypropylene colored with ([phathalocyaninato(2-)] copper). OviTex will incorporate into the recipient tissue with associated cellular and microvascular ingrowth.OviTex is provided in various shapes and sizes to suit surgeon preference and the complexity of the soft tissue repair. The device may be trimmed to a desired shape to further accommodate an individual patient’s requirements.

Device Class : 2

Duns Number: 594540572

Premarket Exempt : No

Product Code : FTL, FTM

Prescription Use : Yes

Device Count : 1

- Catalog Number : F10248-2530P

Device Description : OviTex™ Core Reinforced Tissue Matrix with Permanent Polymer (OviTex) is a steri OviTex™ Core Reinforced Tissue Matrix with Permanent Polymer (OviTex) is a sterile bioscaffold composed of ovine (sheep) derived extracellular matrix (ECM) and monofilament polypropylene colored with ([phathalocyaninato(2-)] copper). OviTex will incorporate into the recipient tissue with associated cellular and microvascular ingrowth.OviTex is provided in various shapes and sizes to suit surgeon preference and the complexity of the soft tissue repair. The device may be trimmed to a desired shape to further accommodate an individual patient’s requirements.

Device Class : 2

Duns Number: 594540572

Premarket Exempt : No

Product Code : FTL, FTM

Prescription Use : Yes

Device Count : 1

- Catalog Number : F10248-2540P

Device Description : OviTex™ Core Reinforced Tissue Matrix with Permanent Polymer (OviTex) is a steri OviTex™ Core Reinforced Tissue Matrix with Permanent Polymer (OviTex) is a sterile bioscaffold composed of ovine (sheep) derived extracellular matrix (ECM) and monofilament polypropylene colored with ([phathalocyaninato(2-)] copper). OviTex will incorporate into the recipient tissue with associated cellular and microvascular ingrowth.OviTex is provided in various shapes and sizes to suit surgeon preference and the complexity of the soft tissue repair. The device may be trimmed to a desired shape to further accommodate an individual patient’s requirements.

Device Class : 2

Duns Number: 594540572

Premarket Exempt : No

Product Code : FTL, FTM

Prescription Use : Yes

Device Count : 1