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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PEEK, TLIF, 26L X 10W X 13H
Altus Spine, LLC
PS-261013
In Commercial Distribution

  • B417PS2610131 ()
  • 00843210118093 ()

  • Angle: 7 degree
  • Height: 13 Millimeter
  • Width: 10 Millimeter
  • Length: 26 Millimeter


  • Polymeric spinal interbody fusion cage
PEEK, TLIF, 26L X 10W X 12H
Altus Spine, LLC
PS-261012
In Commercial Distribution

  • B417PS2610121 ()
  • 00843210118130 ()

  • Angle: 7 degree
  • Width: 10 Millimeter
  • Length: 26 Millimeter
  • Height: 12 Millimeter


  • Polymeric spinal interbody fusion cage
PEEK, TLIF, 26L X 10W X 11H
Altus Spine, LLC
PS-261011
In Commercial Distribution

  • B417PS2610111 ()
  • 00843210118253 ()

  • Length: 26 Millimeter
  • Angle: 7 degree
  • Width: 10 Millimeter
  • Height: 11 Millimeter


  • Polymeric spinal interbody fusion cage
PEEK, TLIF, 26L X 10W X 10H
Altus Spine, LLC
PS-261010
In Commercial Distribution

  • B417PS2610101 ()
  • 00843210118260 ()

  • Length: 26 Millimeter
  • Width: 10 Millimeter
  • Angle: 7 degree
  • Height: 10 Millimeter


  • Polymeric spinal interbody fusion cage
PEEK, TLIF, 26L X 10W X 9H
Altus Spine, LLC
PS-261009
In Commercial Distribution

  • B417PS2610091 ()
  • 00843210118079 ()

  • Angle: 7 degree
  • Length: 26 Millimeter
  • Height: 9 Millimeter
  • Width: 10 Millimeter


  • Polymeric spinal interbody fusion cage
PEEK, TLIF, 26L X 10W X 8H
Altus Spine, LLC
PS-261008
In Commercial Distribution

  • B417PS2610081 ()
  • 00843210118123 ()

  • Height: 8 Millimeter
  • Width: 10 Millimeter
  • Angle: 7 degree
  • Length: 26 Millimeter


  • Polymeric spinal interbody fusion cage
PEEK, TLIF, 26L X 10W X 7H
Altus Spine, LLC
PS-261007
In Commercial Distribution

  • B417PS2610071 ()
  • 00843210118208 ()

  • Angle: 7 degree
  • Height: 7 Millimeter
  • Length: 26 Millimeter
  • Width: 10 Millimeter


  • Polymeric spinal interbody fusion cage
Conformers (made of acrylic or PMMA) are single use devices. They are used to keep the form of the orbital cavity after enucleation or evisceration. In fact, a well chosen conformer enhances healing and prevents retraction of the cul-de-sac. It facilitates the fabrication and the retention of the ocular prosthesis. The conformer temporarily takes the place of the volume lost after enucleation or evisceration and keeps the lids in their natural position. It can be inserted in both eyes (left eye or right eye). The conformer is inserted behind the lids at the end of the surgery and stays in place until the next appointment with the ophthalmologist and/or the ocularist before an ocular prosthesis is made. This period of time varies for each patient and can range between one (1) to four (4) weeks. The conformer is never worn for more than 30 days continuously.
Oculo-Plastik Inc
19-124
Not in Commercial Distribution


  • Length: 26 Millimeter
  • Width: 25.5 Millimeter
  • Depth: 1.8 Millimeter


  • Ophthalmic conformer
Integra® Jarit® VATS Flat Suction Instrument, Variable Suction, Blunt Tip, Curved
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
323913
In Commercial Distribution

  • M2743239131 ()
  • 10381780130284 ()

  • 16-1/2"
  • Length: 11.5 Millimeter
  • Width: 8 Millimeter
323-913

  • Suction system catheter, general-purpose
Integra® Jarit® VATS Flat Suction Instrument, Blunt Tip, Curved
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
323912
In Commercial Distribution

  • M2743239121 ()
  • 10381780130277 ()

  • 16-1/2"
  • Width: 8 Millimeter
  • Length: 11.5 Millimeter
323-912

  • Suction system catheter, general-purpose
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