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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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TRULIANT CC INSRT TOPPER SIZE 4 THICK
Exactech, Inc.
02-029-25-3840
In Commercial Distribution

  • 10885862556981 ()

  • SIZE 4
  • THICK
02-029-25-3840

  • Knee tibia prosthesis trial, reusable
TRULIANT CC INSRT TOPPER SIZE 3 THICK
Exactech, Inc.
02-029-25-3830
In Commercial Distribution

  • 10885862556974 ()

  • THICK
  • SIZE 3
02-029-25-3830

  • Knee tibia prosthesis trial, reusable
TRULIANT CC INSRT TOPPER SIZE 2 THICK
Exactech, Inc.
02-029-25-3820
In Commercial Distribution

  • 10885862556967 ()

  • SIZE 2
  • THICK
02-029-25-3820

  • Knee tibia prosthesis trial, reusable
TRULIANT CC INSRT TOPPER SIZE 1 THICK
Exactech, Inc.
02-029-25-3810
In Commercial Distribution

  • 10885862556950 ()

  • THICK
  • SIZE 1
02-029-25-3810

  • Knee tibia prosthesis trial, reusable
TRULIANT CC INSRT TOPPER SIZE 5 THIN
Exactech, Inc.
02-029-25-3750
In Commercial Distribution

  • 10885862556943 ()

  • THIN
  • SIZE 5
02-029-25-3750

  • Knee tibia prosthesis trial, reusable
TRULIANT CC INSRT TOPPER SIZE 4 THIN
Exactech, Inc.
02-029-25-3740
In Commercial Distribution

  • 10885862556936 ()

  • THIN
  • SIZE 4
02-029-25-3740

  • Knee tibia prosthesis trial, reusable
TRULIANT CC INSRT TOPPER SIZE 3 THIN
Exactech, Inc.
02-029-25-3730
In Commercial Distribution

  • 10885862556929 ()

  • SIZE 3
  • THIN
02-029-25-3730

  • Knee tibia prosthesis trial, reusable
TRULIANT CC INSRT TOPPER SIZE 2 THIN
Exactech, Inc.
02-029-25-3720
In Commercial Distribution

  • 10885862556912 ()

  • SIZE 2
  • THICK
02-029-25-3720

  • Knee tibia prosthesis trial, reusable
TRULIANT CC INSRT TOPPER SIZE 1 THIN
Exactech, Inc.
02-029-25-3710
In Commercial Distribution

  • 10885862556905 ()

  • THIN
  • SIZE 1
02-029-25-3710

  • Knee tibia prosthesis trial, reusable
XATP MIS Penfield Blade, 80mm C-C Right
Nuvasive, Inc.
Z200282-81
In Commercial Distribution

  • 00195377164070 ()


  • Internal spinal fixation procedure kit, reusable
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