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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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CC MOORE ENDO 44MM STER
Smith & Nephew, Inc.
76570344
Not in Commercial Distribution

  • 03596010377166 ()
76570344

  • Metallic femoral head prosthesis
CC MOORE ENDO 43MM STER
Smith & Nephew, Inc.
76570343
Not in Commercial Distribution

  • 03596010377159 ()
76570343

  • Metallic femoral head prosthesis
CC MOORE ENDO 42MM STER
Smith & Nephew, Inc.
76570342
Not in Commercial Distribution

  • 03596010377142 ()
76570342

  • Metallic femoral head prosthesis
CC MOORE ENDO 41MM STER
Smith & Nephew, Inc.
76570341
Not in Commercial Distribution

  • 03596010377135 ()
76570341

  • Metallic femoral head prosthesis
LIF, RASP, CC OFFSET, 22MM
ALPHATEC SPINE, INC.
256-16-100-22
In Commercial Distribution

  • 00190376394411 ()


  • Bone file/rasp, manual, reusable
LIF, RASP, CC OFFSET, 20MM
ALPHATEC SPINE, INC.
256-16-100-20
In Commercial Distribution

  • 00190376394404 ()


  • Bone file/rasp, manual, reusable
LIF, RASP, CC OFFSET, 18MM
ALPHATEC SPINE, INC.
256-16-100-18
In Commercial Distribution

  • 00190376394398 ()


  • Bone file/rasp, manual, reusable
LIF, RASP, CC OFFSET, 16MM
ALPHATEC SPINE, INC.
256-16-100-16
In Commercial Distribution

  • 00190376394381 ()


  • Bone file/rasp, manual, reusable
LIF, RASP, CC OFFSET, 14MM
ALPHATEC SPINE, INC.
256-16-100-14
In Commercial Distribution

  • 00190376394374 ()


  • Bone file/rasp, manual, reusable
LIF, RASP, CC OFFSET, 12MM
ALPHATEC SPINE, INC.
256-16-100-12
In Commercial Distribution

  • 00190376394367 ()


  • Bone file/rasp, manual, reusable
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