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MEDPOR - Stryker MedEd

MEDPORO rbital Floor Illustrations are not actual size. Please consult dimensional in a variety of shapes, sizes, and configurations, MEDPOR and MEDPOR TITANI mplants provide surgeons with an expanding range of options for reconstruction and augmentation of orbital fractures. MEDPOR Biomaterial has been used in over 400,000surgical procedures and referenced in over 350 published articles since 1985. Theinterconnecting, omni-directional pore structure of the biocompatible porous materialmay allow for fibrovascular in-growth and integration of the patient s BARRIER Implants are designed to reduce tissue attachment to the non-porousBARRIER surface of the implants. MEDPOR TITAN was the first craniofacial implant to combine high-density polyethylenesheets and titanium mesh in a single implant for increased flexibility, shape retention,radiographic visualization and Fracture RepairCAT# TITAN FAN Available in two configurations, with or without a BARRIERMTM Titanium mesh embedded within porous, high-density polyethyleneMTB Titanium mesh embedded within a porous polyethylene matrix with a solid,barrier surface on one side, potentially allowing for fibrovascular ingrowth only on the porous side of the implant Combines high-density polyethylene sheets and titanium mesh in a single implant forincreased flexibility, shape retention, radiographic visualization and strength12 CAT#ABTHICKNESS8302038mm Thin SheetsUltra Thin SheetsCAT# are not

Illustrations are not actual size. Please consult dimensional descriptions. Available in a variety of shapes, sizes, and configurations, MEDPOR and MEDPOR TITAN

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Transcription of MEDPOR - Stryker MedEd

1 MEDPORO rbital Floor Illustrations are not actual size. Please consult dimensional in a variety of shapes, sizes, and configurations, MEDPOR and MEDPOR TITANI mplants provide surgeons with an expanding range of options for reconstruction and augmentation of orbital fractures. MEDPOR Biomaterial has been used in over 400,000surgical procedures and referenced in over 350 published articles since 1985. Theinterconnecting, omni-directional pore structure of the biocompatible porous materialmay allow for fibrovascular in-growth and integration of the patient s BARRIER Implants are designed to reduce tissue attachment to the non-porousBARRIER surface of the implants. MEDPOR TITAN was the first craniofacial implant to combine high-density polyethylenesheets and titanium mesh in a single implant for increased flexibility, shape retention,radiographic visualization and Fracture RepairCAT# TITAN FAN Available in two configurations, with or without a BARRIERMTM Titanium mesh embedded within porous, high-density polyethyleneMTB Titanium mesh embedded within a porous polyethylene matrix with a solid,barrier surface on one side, potentially allowing for fibrovascular ingrowth only on the porous side of the implant Combines high-density polyethylene sheets and titanium mesh in a single implant forincreased flexibility, shape retention, radiographic visualization and strength12 CAT#ABTHICKNESS8302038mm Thin SheetsUltra Thin SheetsCAT# are not actual size.

2 Please consult dimensional # are not actual size. Please consult dimensional #DESCRIPTIONABTHICKNESS9527 BARRIER Channel SheetBARRIER Single Channel SheetsCAT#DESCRIPTIONABTHICKNESS9531 BARRIER Miniplate Sheet 9532 BARRIER Sheet BARRIER Channel SheetsCAT#DESCRIPTIONABTHICKNESS8305 Orbital Floor Implant Floor SheetsCAT# DESCRIPTION A BTHICKNESS9541 Regular Regular Right22mm 31mm Large Left 28mm 40mm Large Right28mm40mm Wedge4 Illustrations are not actual size. Please consult dimensional #DESCRIPTIONABCTHICKNESS81034 MTM 41mm 42mm - Left 41mm 42mm - Right 41mm 42mm Patent 7,655,047 MEDPOR TITAN MAX Orbital Floor and Wall (OFW)CAT# Patent 7,655,047 MEDPOR TITAN Orbital Floor and Wall (OFW)CAT# 38mm50mm 76mm50mm 38mm 50mm 76mm 50mm 81026 MTB 38mm 50mm 76mm 38mm 50mm 76mm 50mm TITAN ImplantsMTM- Titanium mesh embedded within porous, high-density Titanium mesh embedded within a porous polyethylene matrix with a solid, barrier surface onone side, potentially allowing for fibrovascular ingrowth only on the porous side of the Titanium mesh embedded within solid, non-porous high-density Australia8 Herbert StreetSt LeonardsNSW 2065 AustraliaPhone: +61 (2) 9467 1000 Fax: +61 (2) 9467 1010 Stryker New Zealand515 Mt.

3 Wellington HighwayAuckland 1060 New ZealandPhone: +64 (9) 573 1890 Fax: +64 (9) 573 document is intended solely for the use of healthcare surgeon must always rely on his or her own professional clinical judgment when deciding whether to use a particular product when treating a particular patient. Strykerdoes not dispense medical advice and recommends that surgeons be trained in the use of any particular product before using it in surgery. The information presented in this brochure is intended to demonstrate a Stryker product. Always refer to thepackage insert, product label and/or user instructions including the instructions for cleaning and sterilization (if applicable)before using any Stryker products. Products may not be available in all markets. Product availability is subject to the regulatoryor medical practices that govern individual markets. Please contact your Stryker representative if you have questions about the availability of Stryker products in your area. This document is not for the distribution in the Corporation or its divisions or other corporate affiliated entities own, use or have applied for the following trademarks or service marks: Strykyer, HydroSet.

4 All other trademarks are trademarks of their respective owners or products listed above are CE Number 9410-400-189-SSPLOT C0214 Copyright 2014 StrykerPrinted in Australia1275


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