Protec Medizintechnik GmbH & Co. KG

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Web: http://www.protec-med.com
E-Mail:
Address: Lichtenberger Str. 35, Oberstenfeld 71720, Germany
Phone: +49-(7062)-92 55 12 | Map/Directions >>
 
 

Profile: Protec Medizintechnik GmbH & Co. KG manufactures X-ray film processors. We deal with the subject of digital systems for medical imaging. Our analog products are X-ray film processors, chemical mixers and its accessories. Our digital products are Proscan CR-system and Promis medical imaging software as well as hardware.

The company has revenues of USD 5-10 Million, has ~30 employees and is ISO 9001, CE certified.

FDA Registration Number: 992818

21 Products/Services (Click for related suppliers)  
• Automatic Radiographic Film Processor (FDA Code: IXW / 892.1900)
An automatic radiographic film processor is a device intended to be used to develop, fix, wash, and dry automatically and continuously film exposed for medical purposes.
• Computed Radiography Accessories
• Computed Radiography Kits
• Dark Room Equipment
• Dark Room Equipment Accessories
• Dark Room Equipment Spare Parts
• Film & Image Processors
• Film Image Accessories
• Film/image Processor Spare Parts
• General Medical Imaging Accessories
• General Medical Imaging Device Spares
• Mammography Accessories
• Mammography Devices
• Mammography Spares
• Medical Imaging
• Medical Imaging Kits
• Metal/Polymer Semi-Constrained Hip Prosthesis (FDA Code: LPH / 888.3358)
A hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis is a device intended to be implanted to replace a hip joint. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across the joint. This generic type of device has a femoral component made of a cobalt-chromium-molybdenum (Co-Cr-Mo) alloy or a titanium-aluminum-vanadium (Ti-6Al-4V) alloy and an acetabular component composed of an ultra-high molecular weight polyethylene articulating bearing surface fixed in a metal shell made of Co-Cr-Mo or Ti-6Al-4V. The femoral stem and acetabular shell have a porous coating made of, in the case of Co-Cr-Mo substrates, beads of the same alloy, and in the case of Ti-6Al-4V substrates, fibers of commercially pure titanium or Ti-6Al-4V alloy. The porous coating has a volume porosity between 30 and 70 percent, an average pore size between 100 and 1,000 microns, interconnecting porosity, and a porous coating thickness between 500 and 1,500 microns. The generic type of device has a design to achieve biological fixation to bone without the use of bone cement.
• Osteophilic Finish Cemented/Non-porous Cemented Semi-constrained Hip Prosthesis (FDA Code: MAY / 888.3353)
A hip joint metal/ceramic/polymer semi-constrained cemented or nonporous uncemented prosthesis is a device intended to be implanted to replace a hip joint. This device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across-the-joint. The two-part femoral component consists of a femoral stem made of alloys to be fixed in the intramedullary canal of the femur by impaction with or without use of bone cement. The proximal end of the femoral stem is tapered with a surface that ensures positive locking with the spherical ceramic (aluminium oxide, A1203) head of the femoral component. The acetabular component is made of ultra-high molecular weight polyethylene or ultra-high molecular weight polyethylene reinforced with nonporous metal alloys, and used with or without bone cement.
• Picture Archiving & Communications Systems
• Picture Archiving System Accessories
• Software Programs

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