SEARCH RESULTS FOR: (*d47 external mil*)(24936 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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SCREW, HEX, RED 2, HALO FIXATION, SMOOTH, SILVER, CP TITANIUM
KLS-Martin L.P.
51-575-12-09
In Commercial Distribution

  • 10888118082289 ()
  • 00888118082282 ()

  • TTL=55 MM


  • Implantable craniofacial bone distractor
SCREW, HEX, RED 2, HALO FIXATION, SMOOTH, SILVER, CP TITANIUM
KLS-Martin L.P.
51-575-10-09
In Commercial Distribution

  • 10888118082265 ()
  • 00888118082268 ()

  • TTL=45 MM


  • Implantable craniofacial bone distractor
No Description
BIOMET MICROFIXATION, INC
SP-1579
In Commercial Distribution

  • 00841036092825 ()
SP-1579

  • Implantable craniofacial bone distractor
5.5mm Rod Cutter
Life Spine, Inc.
113-243
In Commercial Distribution

  • 00190837023737 ()
113-243

  • External orthopaedic fixation system, single-use
Oblique Support
Life Spine, Inc.
172-007
In Commercial Distribution

  • 00190837023720 ()
172-007

  • External orthopaedic fixation system, single-use
Outboard Hinge
Life Spine, Inc.
172-006
In Commercial Distribution

  • 00190837023713 ()
172-006

  • External orthopaedic fixation system, single-use
Inline Hinge
Life Spine, Inc.
172-005
In Commercial Distribution

  • 00190837023706 ()
172-005

  • External orthopaedic fixation system, single-use
Universal Hinge
Life Spine, Inc.
172-004
In Commercial Distribution

  • 00190837023690 ()
172-004

  • External orthopaedic fixation system, single-use
Walker Rail
Life Spine, Inc.
172-001
In Commercial Distribution

  • 00190837023683 ()
172-001

  • External orthopaedic fixation system, single-use
Distraction Nut
Life Spine, Inc.
172-022
In Commercial Distribution

  • 00190837023676 ()
172-022

  • External orthopaedic fixation system, single-use
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