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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 RL SZ 3, 5MM
Exactech, Inc.
02-013-50-3012
In Commercial Distribution

  • 10885862626479 ()
02-013-50-3012

  • Knee tibia prosthesis trial, reusable
TRULIANT FIT AUGMENT TRIAL 1/2 RM SZ 3, 5MM
Exactech, Inc.
02-013-50-3011
In Commercial Distribution

  • 10885862626462 ()
02-013-50-3011

  • Knee tibia prosthesis trial, reusable
TRULIANT FIT AUGMENT TRIAL 1/2 RL SZ 2.5,10MM
Exactech, Inc.
02-013-50-2514
In Commercial Distribution

  • 10885862626455 ()
02-013-50-2514

  • Knee tibia prosthesis trial, reusable
TRULIANT FIT AUGMENT TRIAL 1/2 RM SZ 2.5,10MM
Exactech, Inc.
02-013-50-2513
In Commercial Distribution

  • 10885862626448 ()
02-013-50-2513

  • Knee tibia prosthesis trial, reusable
TRULIANT FIT AUGMENT TRIAL 1/2 RL SZ 2.5, 5MM
Exactech, Inc.
02-013-50-2512
In Commercial Distribution

  • 10885862626431 ()
02-013-50-2512

  • Knee tibia prosthesis trial, reusable
TRULIANT FIT AUGMENT TRIAL 1/2 RM SZ 2.5, 5MM
Exactech, Inc.
02-013-50-2511
In Commercial Distribution

  • 10885862626424 ()
02-013-50-2511

  • Knee tibia prosthesis trial, reusable
TRULIANT FIT AUGMENT TRIAL 1/2 RL SZ 2, 10MM
Exactech, Inc.
02-013-50-2014
In Commercial Distribution

  • 10885862626417 ()
02-013-50-2014

  • Knee tibia prosthesis trial, reusable
TRULIANT FIT AUGMENT TRIAL 1/2 RM SZ 2,10MM
Exactech, Inc.
02-013-50-2013
In Commercial Distribution

  • 10885862626400 ()
02-013-50-2013

  • Knee tibia prosthesis trial, reusable
TRULIANT FIT AUGMENT TRIAL 1/2 RL SZ 2, 5MM
Exactech, Inc.
02-013-50-2012
In Commercial Distribution

  • 10885862626394 ()
02-013-50-2012

  • 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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