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 Type Device Class Implantable

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JOURNEY II CR INSERT TRIAL SZ 1-2 9MM RIGHT
Smith & Nephew, Inc.
74033859
In Commercial Distribution

  • 00885556777206 ()
74033859

  • Knee tibia prosthesis trial, reusable
JOURNEY II CR INSERT TRIAL SZ 7-8 10MM LEFT
Smith & Nephew, Inc.
74033858
In Commercial Distribution

  • 00885556777190 ()
74033858

  • Knee tibia prosthesis trial, reusable
JOURNEY II CR INSERT TRIAL SZ 7-8 9MM LEFT
Smith & Nephew, Inc.
74033857
In Commercial Distribution

  • 00885556777183 ()
74033857

  • Knee tibia prosthesis trial, reusable
JOURNEY II CR INSERT TRIAL SZ 5-6 10MM LEFT
Smith & Nephew, Inc.
74033856
In Commercial Distribution

  • 00885556777176 ()
74033856

  • Knee tibia prosthesis trial, reusable
JOURNEY II CR INSERT TRIAL SZ 5-6 9MM LEFT
Smith & Nephew, Inc.
74033855
In Commercial Distribution

  • 00885556777169 ()
74033855

  • Knee tibia prosthesis trial, reusable
JOURNEY II CR INSERT TRIAL SZ 3-4 10MM LEFT
Smith & Nephew, Inc.
74033854
In Commercial Distribution

  • 00885556777152 ()
74033854

  • Knee tibia prosthesis trial, reusable
JOURNEY II CR INSERT TRIAL SZ 3-4 9MM LEFT
Smith & Nephew, Inc.
74033853
In Commercial Distribution

  • 00885556777145 ()
74033853

  • Knee tibia prosthesis trial, reusable
JOURNEY II CR INSERT TRIAL SZ 1-2 10MM LEFT
Smith & Nephew, Inc.
74033852
In Commercial Distribution

  • 00885556777138 ()
74033852

  • Knee tibia prosthesis trial, reusable
2MM RECUT BLOCK
Smith & Nephew, Inc.
E0016877-2
In Commercial Distribution

  • 00885556776490 ()
E0016877-2

  • Orthopaedic implant aiming/guiding block, reusable
JII XR TIBIA BLOCK 0 DEGREE RIGHT
Smith & Nephew, Inc.
E0016920-2
In Commercial Distribution

  • 00885556779668 ()
E0016920-2

  • Orthopaedic implant aiming/guiding block, reusable
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