SEARCH RESULTS FOR: Femoral(22148 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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DHS®/DCS® ONE-STEP LAG SCREW 12.7MM THREAD/50MM
Synthes GmbH
280.251
In Commercial Distribution

  • H6792802510 ()
  • 10886982174994 ()
280251

  • Orthopaedic bone screw (non-sliding)
Titanium Ridge Augmentation Mesh, 45 mm x 45 mm, Non-sterile
Osteogenics Biomedical Inc
TM4545NS
In Commercial Distribution

  • D765TM4545NS0 ()

  • Length: 45 Millimeter
  • Width: 45 Millimeter


  • Extra-gynaecological surgical mesh, metal
Titanium Ridge Augmentation Mesh, 25 mm x 34 mm, Non-sterile
Osteogenics Biomedical Inc
TM2534NS
In Commercial Distribution

  • D765TM2534NS0 ()

  • Length: 34 Millimeter
  • Width: 25 Millimeter


  • Extra-gynaecological surgical mesh, metal
No Description
Microport Orthopedics Inc.
E351824R
In Commercial Distribution

  • M684E351824R1 ()
  • 00192629249783 ()
E351824R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351824L
In Commercial Distribution

  • M684E351824L1 ()
  • 00192629249776 ()
E351824L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351822R
In Commercial Distribution

  • M684E351822R1 ()
  • 00192629249769 ()
E351822R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351822L
In Commercial Distribution

  • M684E351822L1 ()
  • 00192629249752 ()
E351822L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351820R
In Commercial Distribution

  • M684E351820R1 ()
  • 00192629249745 ()
E351820R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351820L
In Commercial Distribution

  • M684E351820L1 ()
  • 00192629249738 ()
E351820L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351817R
In Commercial Distribution

  • M684E351817R1 ()
  • 00192629249721 ()
E351817R

  • Knee revision prosthesis trial
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