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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Femoral Posterior Augmentation # 2/4mm - Ti6Al4V
Medacta International SA
02.07.7204FPW
In Commercial Distribution

  • 07630971258310 ()


  • Knee arthroplasty wedge
Femoral Posterior Augmentation # 1/8mm - Ti6Al4V
Medacta International SA
02.07.7108FPW
In Commercial Distribution

  • 07630971258303 ()


  • Knee arthroplasty wedge
Femoral Posterior Augmentation # 1/4mm - Ti6Al4V
Medacta International SA
02.07.7104FPW
In Commercial Distribution

  • 07630971258297 ()


  • Knee arthroplasty wedge
UNIVERSAL FEMORAL SLEEVE FULL POROUS 46mm
DEPUY (IRELAND)
1294-53-246
In Commercial Distribution

  • 10603295026365 ()
129453246

  • Knee arthroplasty wedge
UNIVERSAL FEMORAL SLEEVE DISTAL POROUS 46mm
DEPUY (IRELAND)
1294-53-245
In Commercial Distribution

  • 10603295026358 ()
129453245

  • Knee arthroplasty wedge
UNIVERSAL FEMORAL SLEEVE FULL POROUS 40mm
DEPUY (IRELAND)
1294-53-236
In Commercial Distribution

  • 10603295026334 ()
129453236

  • Knee arthroplasty wedge
UNIVERSAL FEMORAL SLEEVE DISTAL POROUS 40mm
DEPUY (IRELAND)
1294-53-235
In Commercial Distribution

  • 10603295026327 ()
129453235

  • Knee arthroplasty wedge
UNIVERSAL FEMORAL SLEEVE FULL POROUS 34mm
DEPUY (IRELAND)
1294-53-226
In Commercial Distribution

  • 10603295026303 ()
129453226

  • Knee arthroplasty wedge
UNIVERSAL FEMORAL SLEEVE DISTAL POROUS 34mm
DEPUY (IRELAND)
1294-53-225
In Commercial Distribution

  • 10603295026297 ()
129453225

  • Knee arthroplasty wedge
UNIVERSAL FEMORAL SLEEVE FULL POROUS 31mm
DEPUY (IRELAND)
1294-53-216
In Commercial Distribution

  • 10603295026273 ()
129453216

  • Knee arthroplasty wedge
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