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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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BOTTOM TRAY, GENERAL DISCECTOMY CASE #2
Orthofix US LLC
26-8222
In Commercial Distribution

  • 18257200126002 ()


  • Metallic spinal interbody fusion cage
TOP TRAY, GENERAL DISCECTOMY CASE #2
Orthofix US LLC
26-8221
In Commercial Distribution

  • 18257200125999 ()


  • Metallic spinal interbody fusion cage
BOTTOM TRAY, GENERAL DISCECTOMY CASE #1
Orthofix US LLC
26-8122
In Commercial Distribution

  • 18257200125982 ()


  • Metallic spinal interbody fusion cage
TOP TRAY, GENERAL DISCECTOMY CASE #1
Orthofix US LLC
26-8121
In Commercial Distribution

  • 18257200125975 ()


  • Metallic spinal interbody fusion cage
CENTURION - BONE SCREW CADDY, OCCIPITAL CASE
Orthofix US LLC
69-8301
In Commercial Distribution

  • 18257200125197 ()


  • Bone-screw internal spinal fixation system, non-sterile
CETRA - BOTTOM TRAY-LEVEL, IMPLANT/INSTRUMENT CASE
Orthofix US LLC
19-1003
In Commercial Distribution

  • 18257200122400 ()


  • Spinal fixation plate, non-bioabsorbable
CETRA - TOP TRAY-LEVEL, IMPLANT/INSTRUMENT CASE
Orthofix US LLC
19-1002
In Commercial Distribution

  • 18257200122394 ()


  • Spinal fixation plate, non-bioabsorbable
LONESTAR - BOTTOM LEVEL, IMPLANT / INSTRUMENT CASE
Orthofix US LLC
83-0104
In Commercial Distribution

  • 18257200118540 ()


  • Metallic spinal interbody fusion cage
LONESTAR - MIDDLE LEVEL, IMPLANT / INSTRUMENT CASE
Orthofix US LLC
83-0103
In Commercial Distribution

  • 18257200118533 ()


  • Metallic spinal interbody fusion cage
LONESTAR - TOP LEVEL, IMPLANT / INSTRUMENT CASE
Orthofix US LLC
83-0102
In Commercial Distribution

  • 18257200118526 ()


  • Metallic spinal interbody fusion cage
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