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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 FIT AUGMENT TRIAL 1/2 RM SZ 6,10MM
Exactech, Inc.
02-013-50-6013
In Commercial Distribution

  • 10885862626684 ()
02-013-50-6013

  • Knee tibia prosthesis trial, reusable
TRULIANT FIT AUGMENT TRIAL 1/2 RL SZ 6, 5MM
Exactech, Inc.
02-013-50-6012
In Commercial Distribution

  • 10885862626677 ()
02-013-50-6012

  • Knee tibia prosthesis trial, reusable
TRULIANT FIT AUGMENT TRIAL 1/2 RM SZ 6, 5MM
Exactech, Inc.
02-013-50-6011
In Commercial Distribution

  • 10885862626660 ()
02-013-50-6011

  • Knee tibia prosthesis trial, reusable
TRULIANT FIT AUGMENT TRIAL 1/2 RM SZ 5, 10MM
Exactech, Inc.
02-013-50-5013
In Commercial Distribution

  • 10885862626646 ()
02-013-50-5013

  • Knee tibia prosthesis trial, reusable
TRULIANT FIT AUGMENT TRIAL 1/2 RM SZ 5, 5MM
Exactech, Inc.
02-013-50-5011
In Commercial Distribution

  • 10885862626622 ()
02-013-50-5011

  • Knee tibia prosthesis trial, reusable
TRULIANT FIT AUGMENT TRIAL 1/2 RL SZ 4.5,10MM
Exactech, Inc.
02-013-50-4514
In Commercial Distribution

  • 10885862626615 ()
02-013-50-4514

  • Knee tibia prosthesis trial, reusable
TRULIANT FIT AUGMENT TRIAL 1/2 RM SZ 4.5,10MM
Exactech, Inc.
02-013-50-4513
In Commercial Distribution

  • 10885862626608 ()
02-013-50-4513

  • Knee tibia prosthesis trial, reusable
TRULIANT FIT AUGMENT TRIAL 1/2 RL SZ 4.5, 5MM
Exactech, Inc.
02-013-50-4512
In Commercial Distribution

  • 10885862626592 ()
02-013-50-4512

  • Knee tibia prosthesis trial, reusable
TRULIANT FIT AUGMENT TRIAL 1/2 RL SZ 4, 10MM
Exactech, Inc.
02-013-50-4014
In Commercial Distribution

  • 10885862626578 ()
02-013-50-4014

  • Knee tibia prosthesis trial, reusable
TRULIANT FIT AUGMENT TRIAL 1/2 RM SZ 2, 5MM
Exactech, Inc.
02-013-50-2011
In Commercial Distribution

  • 10885862626387 ()
02-013-50-2011

  • Knee tibia prosthesis trial, reusable
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