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 DEG 40/60
Smith & Nephew, Inc.
E0017173-6
In Commercial Distribution

  • 00885556796214 ()
E0017173-6

  • Femoral head prosthesis trial
R3 SCREW-IN TRIAL LINER 0 DEG 40/60
Smith & Nephew, Inc.
E0017173-3
In Commercial Distribution

  • 00885556796184 ()
E0017173-3

  • Femoral head prosthesis trial
32MM +16 TRIAL FEM HEAD - SUTURE HOLE
Smith & Nephew, Inc.
E0016936-12
In Commercial Distribution

  • 00885556780534 ()
E0016936-12

  • Femoral head prosthesis trial
32MM +12 TRIAL FEM HEAD - SUTURE HOLE
Smith & Nephew, Inc.
E0016936-11
In Commercial Distribution

  • 00885556780527 ()
E0016936-11

  • Femoral head prosthesis trial
32MM +8 TRIAL FEM HEAD - SUTURE HOLE
Smith & Nephew, Inc.
E0016936-10
In Commercial Distribution

  • 00885556780510 ()
E0016936-10

  • Femoral head prosthesis trial
32MM +4 TRIAL FEM HEAD - SUTURE HOLE
Smith & Nephew, Inc.
E0016936-9
In Commercial Distribution

  • 00885556780503 ()
E0016936-9

  • Femoral head prosthesis trial
32MM 0 TRIAL FEM HEAD - SUTURE HOLE
Smith & Nephew, Inc.
E0016936-8
In Commercial Distribution

  • 00885556780497 ()
E0016936-8

  • Femoral head prosthesis trial
32MM -3 TRIAL FEM HEAD - SUTURE HOLE
Smith & Nephew, Inc.
E0016936-7
In Commercial Distribution

  • 00885556780480 ()
E0016936-7

  • Femoral head prosthesis trial
28MM +16 TRIAL FEM HEAD - SUTURE HOLE
Smith & Nephew, Inc.
E0016936-6
In Commercial Distribution

  • 00885556780473 ()
E0016936-6

  • Femoral head prosthesis trial
28MM +12 TRIAL FEM HEAD - SUTURE HOLE
Smith & Nephew, Inc.
E0016936-5
In Commercial Distribution

  • 00885556780466 ()
E0016936-5

  • Femoral head prosthesis trial
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