MEDPOR TITAN 3D Orbital Floor Anatomic Implants designed using CT-scan data to approximate the anatomy of the orbital floor & medial wall to enhance the effectiveness and efficiency of reconstruction Proven MEDPOR is a clinically proven material with over 400,000 procedures performed, and more than 350 published clinical reports Smooth

Our technique using the Medpor Titan implant is a fast and effective method for pterional reconstruction after FT and OZ craniotomy with excellent cosmetic results and patient satisfaction. The implant combines the advantages of both porous polyethylene and titanium mesh, including easy custom-shaping without sharp edges, structural support and relatively lower cost.

A patient with this device can be scanned safely under the following conditions: Status magnetic field of 1.5 or 3.0 Tesla; Maximum spatial gradient magnetic field of 720-Gauss/cm (7200-mT/m) or less; Each patient will receive a device ID card following implant. First introduced in 1991 by Dr. John Reinisch, MEDPOR ear reconstruction is a surgical technique used for microtia patients that uses a synthetic framework and the body's own tissue to create an ear. Dr. Reinisch is a leader in this ear reconstruction technique. Important safety information regarding the Medical Procedures for MED‑EL Implant Systems, Bone Conduction Implant System - BCI 601, Middle Ear Implant System - VORP 502, Middle Ear Implant System - VORP 503, and MRI Safety. 17 Sep 2016 Platinum and gold eyelid weights are considered MRI compatible but may also cause susceptibility Medpor ocular implant after evisceration. 15 Jan 2015 Currently used orbital implants are all MR imaging safe.

MRI Information MRI Safety Information MR Conditional Non-clinical testing demonstrated that the LAA Exclusion System clip is MR Conditional. A patient with this device can be scanned safely in an MR system immediately after placement under the following conditions: • Static magnetic field of 1.5-Tesla and 3-Tesla, only SYNPOR ® Porous Polyethylene Implants are ideal for craniofacial reconstruction and augmentation. SYNPOR Polyethylene Implants are manufactured from an inert, nonabsorbable polymer formulated to contain a network of open and interconnecting pores approximately 100 – 250 µm in size. The pores allow for fibrovascular tissue ingrowth.

2020-10-12 · Brand Name: MEDPOR TITAN. Version or Model: 81042. Commercial Distribution Status: In Commercial Distribution. Catalog Number: 81042. Company Name: Stryker Leibinger GmbH & Co. KG. Primary DI Number: 07613327123210. Issuing Agency: GS1. Commercial Distribution End Date: Device Count: 1.

A patient with this device can be safely scanned immediately after placement of the coils in an MR system meeting the following conditions: Implant-related infections usually occur within the first 2 weeks of surgery and have been reported to occur in 3.2% of nasal dorsum implants, 3.8% of malar implants, and 5.3% of chin implants.31,32 Proplast (Vitek, Valencia, California) Teflon (Dupont, Wilmington, Delaware), which is an ultrap-orous composite material, has fallen out of use Features: The plate may extend beyond both ends of the implant, if desired. The implant, with plate in position, allows the surgeon to bend and contour the material to the desired shape. The plates can be used to cantilever the implant over the orbital rim, if applicable.

MRI Information MRI Safety Information MR Conditional Non-clinical testing demonstrated that the LAA Exclusion System clip is MR Conditional. A patient with this device can be scanned safely in an MR system immediately after placement under the following conditions: • Static magnetic field of 1.5-Tesla and 3-Tesla, only

0.2, 1.5. Conditional 5 More Cochlear Implants, MED-EL Corporation More MED-EL CONCERT or CONCERT PIN Cochlear Implant. Med-El, www.medel.com/us/isi-cochlear-implant-systems. 0.2,1.5.

The omni-directional pore A: The porous architecture of the Bio-Eye® hydroxyapatite implant is well implant vascularization with a confirmatory magnetic resonance imaging (MRI) study, A standard spherical Medpor® implant costs approximately $200 (USD) les 31 Jan 2013 removed in 1958. The doctor placed an implant in the socket at that time. If the implant is not metallic, MRI scanning should not present a problem. If metallic Is it safe to have an MRI after cataract surgery? 31 Oct 2008 This value was used at determining the implant size during the operation.
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Orbital Fracture Repair CAT# DESCRIPTION A B THICKNESS 81049 MTM 40mm 62mm 0.85mm 81050 MTB 40mm 62mm 1.0mm MEDPOR TITAN FAN • MEDPOR surgical implants are provided sterile and should not be resterilized. • Do not place or carve the implant on surgical drapes, surgical clothing or any other surface that may contaminate the implant with lint and other particulate matter. The omni-directional pore structure of our polyethylene implants may increase implant acceptance by allowing the patient‘s native tissue to integrate with the implant. In addition to our comprehensive line of stock MEDPOR implants, we offer CT-based patient specific implants, putting the implant design in your hands.

The implant, with plate in position, allows the surgeon to bend and contour the material to the desired shape. The plates can be used to cantilever the implant over the orbital rim, if applicable.
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The omni-directional pore structure of our polyethylene implants may increase implant acceptance by allowing the patient‘s native tissue to integrate with the implant. In addition to our comprehensive line of stock MEDPOR implants, we offer CT-based patient-specific implants , putting the implant design in your hands.

Miscellaneous and Uncommon Devices Boston Keratoprosthesis (MRI Conditional) • The MEDPOR TITAN MEDPOR (MTM) Implant is porous, high-density polyethylene with titanium mesh embedded in it, potentially providing the advantages of fibrovascular integration of the patient’s host tissue through the sheet.2 • The MEDPOR TITAN BARRIER (MTB) Implant is a sheet of titanium mesh embedded within a porous Safety Topic / Subject. MED-EL COMBI 40+ Cochlear Implant System. MED-EL Corporation, www.medel.com.

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Several types of penile implants and prostheses have been evaluated for magnetic field interactions associated with MR systems. Of these, two (i.e., the Duraphase and Omniphase models) demonstrated su

You can trust your by implants from a Straumann® Dental Implant System extends approximately 10 mm from this device when imaged with a gradient echo pulse sequence and a 3 Tesla MR system. English MRI Safety Information The FDA warns of serious adverse events related to medication dosing inaccuracies associated with Implantable Infusion Pumps in the Magnetic Resonance (MR) Environment. The Medpor/Supor implant is then covered with a large, thin membrane (called temporoparietal fascia flap) which is located above the ear in the temple area. This flap is elevated by first undermining a scalp pocket from above the ear. The flap is then brought down to fully cover the medpor/supor implant. The CardioMEMS™ PA Sensor is MRI conditionally approved for 1.5 or 3.0 Tesla imaging. A patient with this device can be scanned safely under the following conditions: Status magnetic field of 1.5 or 3.0 Tesla; Maximum spatial gradient magnetic field of 720-Gauss/cm (7200-mT/m) or less; Each patient will receive a device ID card following implant.

2004-05-01 · The Medpor™ sheet can be an optimal implant to reconstruct the sellar floor or the sphenoid rostrum in endonasal transsphenoidal surgery because of its flexibility and maneuverability, stiffness as a buttress, MR compatibility and the characteristics in the MRI, and biocompatibility.

0.2, 1.5. Conditional 5 More Cochlear Implants, MED-EL Corporation More MED-EL CONCERT or CONCERT PIN Cochlear Implant. Med-El, www.medel.com/us/isi-cochlear-implant-systems. 0.2,1.5.

MEDPOR BARRIER Implants MEDPOR BARRIER Implants are designed to prevent tissue attachment to the implant surface. The BARRIER is made of non-porous, high-density polyethylene and heat bonded to the porous material without adhesives or additives. The porous side of the implant is designed to provide a MEDPOR TITAN was the first craniofacial implant to combine high-density polyethylene sheets and titanium mesh in a single implant for increased flexibility, shape retention, radiographic visualization and strength.1. Orbital Fracture Repair CAT# DESCRIPTION A B THICKNESS 81049 MTM 40mm 62mm 0.85mm 81050 MTB 40mm 62mm 1.0mm MEDPOR TITAN FAN • MEDPOR surgical implants are provided sterile and should not be resterilized. • Do not place or carve the implant on surgical drapes, surgical clothing or any other surface that may contaminate the implant with lint and other particulate matter. The omni-directional pore structure of our polyethylene implants may increase implant acceptance by allowing the patient‘s native tissue to integrate with the implant.