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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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Training electrodes, used for Nevisense training and qualification. Each electrode is to be used only on intact, healthy skin on a single person in a single training session. Each electrode can be used up to 50 times. The reason for the higher number (i.e., 50, as compared with 20 for the examination electrode) is that these electrodes are used for training and qualification purposes only.
Scibase AB
131-0008
In Commercial Distribution

  • 07350094440217 ()
131-0008

  • Neoplasm electrical impedance spectrometer electrode array
Genius AI® is a computer-aided detection and diagnosis (CADe/CADx) software device intended to be used with compatible digital breast tomosynthsis (DBT) systems to identify and mark regions of interest including soft tissue densities (masses, architectural distortions, and assymetries) and calcifications in DBT exams from compatible DBT systems and provide confidence scores that offer assessment for Certainty of Findings and a Case Score.
Hologic, Inc.
GENIUS AI DETECTION SOFTWARE
In Commercial Distribution

  • 15420045512474 ()
ASY-15431

  • Stationary mammographic x-ray system, digital
Paragon RG-4 contact lenses are manufactured from Paragon HDS® 100. The reverse geometry design has a posterior surface consisting of four zones: The central spherical or aspheric zone, an annular “Reverse Zone(s)”surrounding the central zone with a curvature steeper (shorter radius) than the central zone, an “Alignment Zone(s)” generally paralleling the underlying corneal surface and peripheral curve(s) with a radius selected to create “edge lift” to promote tear flow under the lens and avoid impingement of the peripheral curve on the cornea. The lens design also includes a “rounded” edge terminus extending from the anterior to the posterior surfaces to promote comfort. Paragon RG-4 Contact Lenses for Corneal Reshaping are to be worn overnight with removal during all or part of each following day. The material is a thermoset fluorosilicone acrylate copolymer derived primarily from siloxane acrylate, trifluoroethyl methacrylate and methylmethacrylate with a water content of less than 1%. These contact lenses for corneal reshaping are available as lathe cut firm contact lenses with blue, green, red and yellow tints containing D&C Green No. 6, D&C Red No. 17 and Perox Yellow No. 9 (4-[(2,4-dimethylphenyl)azo]-2,4-dihydro-5-methyl-2-phenyl-3H-pyrazol-3-one). These products may be plasma treated.
Paragon Vision Sciences, Inc.
Paragon RG-4
In Commercial Distribution

  • B22220 ()


  • Orthokeratology contact lens
The Model 1680 Torque Wrench is a sterile standard surgical wrench provided for use during the implant procedure to tighten the set screws that secure the leads to the Rechargeable Neuroregulator.
Reshape Lifesciences Inc.
1680
Not in Commercial Distribution

  • 00857334004248 ()

  • Length: 1.685 Inch
  • Outer Diameter: 0.218 Inch
1680

  • Surgical torque wrench, reusable
The Cordella Pulmonary Artery Sensor System is designed for on-demand measurement of pulmonary artery pressure from the patient’s home. Cordella Sensor Delivery Kit consists of the Cordella PA Sensor and Delivery System which are components of the Cordella Pulmonary Artery Sensor System. Cordella PA Sensor The Cordella Sensor is a small implant that resides permanently in the patient’s right pulmonary artery. The Cordella Sensor does not contain batteries or active electrical components. The Cordella Sensor is not made with natural rubber latex. Delivery System The Delivery System is a catheter with a pre-loaded Cordella Sensor at the distal end and is used to implant the Cordella Sensor into the right pulmonary artery. The Delivery System comprises a stability sheath, torque catheter, handle, torque luer, and side port. Implantation of the Cordella Sensor using the Delivery System is designed to be performed during right heart catheterization through venous access. The Stability Sheath contains a marker band at the distal end to aid in visualization under fluoroscopy. The Delivery System is not made with natural rubber latex.
Endotronix, Inc.
100303-05
In Commercial Distribution

  • 00850008997006 ()


  • Implantable pulmonary artery pressure monitoring system
No Description
MEDINOL LTD.
NXL40015US
In Commercial Distribution

  • 07290107012980 ()

  • Length: 15 Millimeter
  • Outer Diameter: 4.0 Millimeter


  • Bare-metal coronary artery stent
No Description
MEDINOL LTD.
NXL35015US
In Commercial Distribution

  • 07290107012973 ()

  • Length: 15 Millimeter
  • Outer Diameter: 3.5 Millimeter


  • Bare-metal coronary artery stent
No Description
MEDINOL LTD.
NXL30015US
In Commercial Distribution

  • 07290107012966 ()

  • Length: 15 Millimeter
  • Outer Diameter: 3.0 Millimeter


  • Bare-metal coronary artery stent
No Description
MEDINOL LTD.
NXL27515US
In Commercial Distribution

  • 07290107012959 ()

  • Length: 15 Millimeter
  • Outer Diameter: 2.75 Millimeter


  • Bare-metal coronary artery stent
No Description
MEDINOL LTD.
NXL25015US
In Commercial Distribution

  • 07290107012942 ()

  • Outer Diameter: 2.50 Millimeter
  • Length: 15 Millimeter


  • Bare-metal coronary artery stent
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