SEARCH RESULTS FOR: ("安卓應用加密[Contact Telegram: Heimaapp].ucb")(4912 results)

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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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GENESIS II FULL TIBIAL WEDGE SIZE 5-6 5MM
Smith & Nephew, Inc.
71925049
In Commercial Distribution

  • 03596010411778 ()
71925049

  • Knee arthroplasty wedge
GENESIS II FULL TIBIAL WEDGE SIZE 3-4 10MM
Smith & Nephew, Inc.
71925048
In Commercial Distribution

  • 03596010411761 ()
71925048

  • Knee arthroplasty wedge
GEN II FULL TIBIAL WEDGE SIZE 3-4 5MM
Smith & Nephew, Inc.
71925047
In Commercial Distribution

  • 03596010411754 ()
71925047

  • Knee arthroplasty wedge
GENISIS UNI TIBIA MODULAR PEG
Smith & Nephew, Inc.
725557
In Commercial Distribution

  • 03596010256843 ()
725557

  • Knee arthroplasty wedge
PROFIX POROUS DISTAL ONLY FEMORAL WEDGE S2 SMALL
Smith & Nephew, Inc.
71500023
Not in Commercial Distribution

  • 03596010436368 ()
71500023

  • Knee arthroplasty wedge
Fem Augment Posterior Sz 6 2mm
Ortho Development Corporation
568-2602
In Commercial Distribution

  • 00822409039999 ()

  • Height: 2 Millimeter


  • Knee arthroplasty wedge
Fem Augment Posterior Sz 5 2mm
Ortho Development Corporation
568-2502
In Commercial Distribution

  • 00822409039982 ()

  • Height: 2 Millimeter


  • Knee arthroplasty wedge
Fem Augment Posterior Sz 4 2mm
Ortho Development Corporation
568-2402
In Commercial Distribution

  • 00822409039975 ()

  • Height: 2 Millimeter


  • Knee arthroplasty wedge
Fem Augment Posterior Sz 3 2mm
Ortho Development Corporation
568-2302
In Commercial Distribution

  • 00822409039968 ()

  • Height: 2 Millimeter


  • Knee arthroplasty wedge
Fem Augment Posterior Sz 2 2mm
Ortho Development Corporation
568-2202
In Commercial Distribution

  • 00822409039951 ()

  • Height: 2 Millimeter


  • Knee arthroplasty wedge
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