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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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No Description
BIOMET MICROFIXATION, INC
SP-2209L
Not in Commercial Distribution

  • 00841036173159 ()
SP-2209L

  • Craniofacial fixation plate, non-bioabsorbable, non-customized
No Description
BIOMET MICROFIXATION, INC
SP-2219R
Not in Commercial Distribution

  • 00841036173142 ()
SP-2219R

  • Craniofacial fixation plate, non-bioabsorbable, non-customized
No Description
BIOMET MICROFIXATION, INC
SP-3084
Not in Commercial Distribution

  • 00841036173067 ()
SP-3084

  • Craniofacial fixation plate, non-bioabsorbable, non-customized
No Description
BIOMET MICROFIXATION, INC
SP-3083
Not in Commercial Distribution

  • 00841036173050 ()
SP-3083

  • Craniofacial fixation plate, non-bioabsorbable, non-customized
No Description
BIOMET MICROFIXATION, INC
SP-3082
Not in Commercial Distribution

  • 00841036173043 ()
SP-3082

  • Craniofacial fixation plate, non-bioabsorbable, non-customized
No Description
BIOMET MICROFIXATION, INC
SP-3081
Not in Commercial Distribution

  • 00841036173036 ()
SP-3081

  • Craniofacial fixation plate, non-bioabsorbable, non-customized
No Description
BIOMET MICROFIXATION, INC
SP-3080
Not in Commercial Distribution

  • 00841036173029 ()
SP-3080

  • Craniofacial fixation plate, non-bioabsorbable, non-customized
No Description
BIOMET MICROFIXATION, INC
SP-3079
Not in Commercial Distribution

  • 00841036173012 ()
SP-3079

  • Craniofacial fixation plate, non-bioabsorbable, non-customized
TRITON,T50 DRIVER,V2 PWE
Choice Spine, LP
Q070-0024
In Commercial Distribution

  • 00840996192866 ()


  • Sacroiliac joint transarticular fixation/arthrodesis implant, uncoated
NAVIGATION,TRITON DRVR V2,NVL
Choice Spine, LP
NV70-Q007
In Commercial Distribution

  • 00840996192750 ()


  • Orthopaedic implant driver
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