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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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Rod Bender, In-Situ, Left
AMEDICA CORPORATION
B
Not in Commercial Distribution

  • M555504000002 ()
50-4000-002

  • Manual orthopaedic bender, reusable
Driver, Polyaxial, Reduction, Long
AMEDICA CORPORATION
B
Not in Commercial Distribution

  • M555503000009 ()
50-3000-009

  • Internal spinal fixation procedure kit, reusable
Driver, Polyaxial, Long
AMEDICA CORPORATION
B
Not in Commercial Distribution

  • M555503000008 ()
50-3000-008

  • Internal spinal fixation procedure kit, reusable
Probe, Lenke, Straight
AMEDICA CORPORATION
B
Not in Commercial Distribution

  • M555502000006 ()
50-2000-006

  • Internal spinal fixation procedure kit, reusable
Probe, Lenke, Curved
AMEDICA CORPORATION
B
Not in Commercial Distribution

  • M555502000005 ()
50-2000-005

  • Internal spinal fixation procedure kit, reusable
Probe, Pedicle, Straight, Duckbill
AMEDICA CORPORATION
B
Not in Commercial Distribution

  • M555502000004 ()
50-2000-004

  • Internal spinal fixation procedure kit, reusable
Probe, Pedicle, Curved, Duckbill
AMEDICA CORPORATION
B
Not in Commercial Distribution

  • M555502000003 ()
50-2000-003

  • Internal spinal fixation procedure kit, reusable
Probe, Sounder, Straight
AMEDICA CORPORATION
B
Not in Commercial Distribution

  • M555502000002 ()
50-2000-002

  • Internal spinal fixation procedure kit, reusable
K-Wire - Nitinol
AMEDICA CORPORATION
B
Not in Commercial Distribution

  • M555501000002 ()
50-1000-002

  • Internal spinal fixation procedure kit, reusable
Valeo PL, 9x25 , 6°, 15mm with Alternative Texture
AMEDICA CORPORATION
B
Not in Commercial Distribution

  • M555110133615 ()

  • Height: 15 Millimeter
  • Width: 25 Millimeter
  • Length: 9 Millimeter
11.013.3615

  • Ceramic spinal interbody fusion cage
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