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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R3 SCREW-IN TRIAL LINER 20¿2/50
Smith & Nephew, Inc.
E0015228-9
In Commercial Distribution

  • 00885556663684 ()
E0015228-9

  • Femoral head prosthesis trial
R3 SCREW-IN TRIAL LINER 20¿2/48
Smith & Nephew, Inc.
E0015228-8
In Commercial Distribution

  • 00885556663677 ()
E0015228-8

  • Femoral head prosthesis trial
R3 SCREW-IN TRIAL LINER 0¿6/60
Smith & Nephew, Inc.
E0015228-7
In Commercial Distribution

  • 00885556663660 ()
E0015228-7

  • Femoral head prosthesis trial
R3 SCREW-IN TRIAL LINER 0¿6/58
Smith & Nephew, Inc.
E0015228-6
In Commercial Distribution

  • 00885556663653 ()
E0015228-6

  • Femoral head prosthesis trial
R3 SCREW-IN TRIAL LINER 0¿6/56
Smith & Nephew, Inc.
E0015228-5
In Commercial Distribution

  • 00885556663646 ()
E0015228-5

  • Femoral head prosthesis trial
R3 SCREW-IN TRIAL LINER 0¿6/54
Smith & Nephew, Inc.
E0015228-4
In Commercial Distribution

  • 00885556663639 ()
E0015228-4

  • Femoral head prosthesis trial
R3 SCREW-IN TRIAL LINER 0¿6/52
Smith & Nephew, Inc.
E0015228-3
In Commercial Distribution

  • 00885556663622 ()
E0015228-3

  • Femoral head prosthesis trial
R3 SCREW-IN TRIAL LINER 0¿2/50
Smith & Nephew, Inc.
E0015228-2
In Commercial Distribution

  • 00885556663615 ()
E0015228-2

  • Femoral head prosthesis trial
R3 SCREW-IN TRIAL LINER 0¿2/48
Smith & Nephew, Inc.
E0015228-1
In Commercial Distribution

  • 00885556663608 ()
E0015228-1

  • Femoral head prosthesis trial
TANDEM STYLE POLAR TRIAL INSERT 53MM X 28MM
Smith & Nephew, Inc.
E0014780-6
Not in Commercial Distribution

  • 00885556618516 ()
E0014780-6

  • Femoral head prosthesis trial
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