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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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Small Hudson PLIF Trial 13x9x24
NEXUS SPINE, L.L.C.
822922
In Commercial Distribution

  • B6788229220 ()
  • B678822922 ()

  • Width: 9 Millimeter
  • Length: 24 Millimeter
  • Height: 13 Millimeter


  • Surgical implant template, reusable
Small Hudson PLIF Trial 12x9x24
NEXUS SPINE, L.L.C.
822921
In Commercial Distribution

  • B6788229210 ()
  • B678822921 ()

  • Width: 9 Millimeter
  • Length: 24 Millimeter
  • Height: 12 Millimeter


  • Surgical implant template, reusable
Small Hudson PLIF Trial 11x9x24
NEXUS SPINE, L.L.C.
822920
In Commercial Distribution

  • B6788229200 ()
  • B678822920 ()

  • Width: 9 Millimeter
  • Length: 24 Millimeter
  • Height: 11 Millimeter


  • Surgical implant template, reusable
Small Hudson PLIF Trial 10x9x24
NEXUS SPINE, L.L.C.
822919
In Commercial Distribution

  • B6788229190 ()
  • B678822919 ()

  • Width: 9 Millimeter
  • Length: 24 Millimeter
  • Height: 10 Millimeter


  • Surgical implant template, reusable
Small Hudson PLIF Trial 9x9x24
NEXUS SPINE, L.L.C.
822918
In Commercial Distribution

  • B6788229180 ()
  • B678822918 ()

  • Width: 9 Millimeter
  • Length: 24 Millimeter
  • Height: 9 Millimeter


  • Surgical implant template, reusable
Small Hudson PLIF Trial 8x9x24
NEXUS SPINE, L.L.C.
822917
In Commercial Distribution

  • B6788229170 ()
  • B678822917 ()

  • Width: 9 Millimeter
  • Length: 24 Millimeter
  • Height: 8 Millimeter


  • Surgical implant template, reusable
Small Hudson PLIF Trial 7x9x24
NEXUS SPINE, L.L.C.
822916
In Commercial Distribution

  • B6788229160 ()
  • B678822916 ()

  • Width: 9 Millimeter
  • Length: 24 Millimeter
  • Height: 7 Millimeter


  • Surgical implant template, reusable
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
19-122
Not in Commercial Distribution


  • Length: 24 Millimeter
  • Width: 23.5 Millimeter
  • Depth: 1.8 Millimeter


  • Ophthalmic conformer
PLIF Trial 17x9x24
NEXUS SPINE, L.L.C.
822176
In Commercial Distribution

  • B6788221760 ()
  • B678822176 ()

  • Width: 9 Millimeter
  • Length: 24 Millimeter
  • Height: 17 Millimeter


  • Surgical implant template, reusable
PLIF Trial 15x9x24
NEXUS SPINE, L.L.C.
822174
In Commercial Distribution

  • B6788221740 ()
  • B678822174 ()

  • Width: 9 Millimeter
  • Length: 24 Millimeter
  • Height: 15 Millimeter


  • Surgical implant template, reusable
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