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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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LID, BASE, CRANIOXPAND
KLS-Martin L.P.
CTM-2303-105
In Commercial Distribution

  • 00888118142986 ()


  • Surgical instrument/implant rack
DIST, MANDIBLE, MICRO ZURICH 2, END DRV, SQUARE MESH, 1.0-1.2 MM SCREW, TI-6AL-4V
KLS-Martin L.P.
02-300-20-09
Not in Commercial Distribution

  • 00888118069344 ()

  • 20 MM, 36 HOLE


  • Implantable craniofacial bone distractor
DIST, MANDIBLE, MICRO ZURICH 2, END DRV, SQUARE MESH, 1.0-1.2 MM SCREW, TI-6AL-4V
KLS-Martin L.P.
02-300-15-09
Not in Commercial Distribution

  • 00888118066374 ()

  • 15 MM, 36 HOLE


  • Implantable craniofacial bone distractor
No Description
I3 IMPLANT LLC
I3PHB
In Commercial Distribution

  • 00810027862471 ()


  • Dental implant suprastructure, temporary, custom-made
No Description
I3 IMPLANT LLC
I3NONH
In Commercial Distribution

  • 00810027862464 ()


  • Dental implant suprastructure, temporary, custom-made
No Description
I3 IMPLANT LLC
I3PH
In Commercial Distribution

  • 00810027862457 ()


  • Dental implant suprastructure, temporary, custom-made
No Description
I3 IMPLANT LLC
I3ANTSMU
In Commercial Distribution

  • 00810027862440 ()


  • Dental implant suprastructure, temporary, custom-made
No Description
I3 IMPLANT LLC
I3ANTRMU
In Commercial Distribution

  • 00810027862433 ()


  • Dental implant suprastructure, temporary, custom-made
No Description
I3 IMPLANT LLC
I3ANAMU
In Commercial Distribution

  • 00810027862426 ()


  • Dental implant suprastructure, temporary, custom-made
No Description
I3 IMPLANT LLC
I3ANFSMU
In Commercial Distribution

  • 00810027862419 ()


  • Dental implant suprastructure, temporary, custom-made
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