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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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Paddle Distractor, 13mm
AMEDICA CORPORATION
K
Not in Commercial Distribution

  • M555910013213 ()
91.001.3213

  • Internal spinal fixation procedure kit, reusable
Paddle Distractor, 12mm
AMEDICA CORPORATION
K
Not in Commercial Distribution

  • M555910013212 ()
91.001.3212

  • Internal spinal fixation procedure kit, reusable
Paddle Distractor, 11mm
AMEDICA CORPORATION
K
Not in Commercial Distribution

  • M555910013211 ()
91.001.3211

  • Internal spinal fixation procedure kit, reusable
Paddle Distractor, 10mm
AMEDICA CORPORATION
K
Not in Commercial Distribution

  • M555910013210 ()
91.001.3210

  • Internal spinal fixation procedure kit, reusable
Paddle Distractor, 9mm
AMEDICA CORPORATION
K
Not in Commercial Distribution

  • M555910013209 ()
91.001.3209

  • Internal spinal fixation procedure kit, reusable
Paddle Distractor, 8mm
AMEDICA CORPORATION
K
Not in Commercial Distribution

  • M555910013208 ()
91.001.3208

  • Internal spinal fixation procedure kit, reusable
Paddle Distractor, 7mm
AMEDICA CORPORATION
K
Not in Commercial Distribution

  • M555910013207 ()
91.001.3207

  • Internal spinal fixation procedure kit, reusable
Taurus Pedicle Screw System- Straight Rod Ext Hex 5.5x600
AMEDICA CORPORATION
K
Not in Commercial Distribution

  • M555252201600 ()

  • Outer Diameter: 5.5 Millimeter
  • Length: 600 Millimeter
25-2201-600

  • Bone-screw internal spinal fixation system rod
Ø6.0mm, In-Situ Rod Bender, LH Shown, RH Opposite
AMEDICA CORPORATION
K
Not in Commercial Distribution

  • M555114000002 ()
11-4000-002

  • Manual orthopaedic bender, reusable
Ø6.0mm, In-Situ Rod Bender, LH Shown, RH Opposite
AMEDICA CORPORATION
K
Not in Commercial Distribution

  • M555114000003 ()
11-4000-003

  • Manual orthopaedic bender, reusable
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