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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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RELINE MAS Trauma Screw, 6.0x110mm Cann
Nuvasive, Inc.
16086011
In Commercial Distribution

  • 00887517559456 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 6.0x100mm Cann
Nuvasive, Inc.
16086010
In Commercial Distribution

  • 00887517559449 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 5.5x95mm Cann
Nuvasive, Inc.
16085595
In Commercial Distribution

  • 00887517559432 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 5.5x90mm Cann
Nuvasive, Inc.
16085590
In Commercial Distribution

  • 00887517559425 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 5.5x85mm Cann
Nuvasive, Inc.
16085585
In Commercial Distribution

  • 00887517559418 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 5.5x80mm Cann
Nuvasive, Inc.
16085580
In Commercial Distribution

  • 00887517559401 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 5.5x75mm Cann
Nuvasive, Inc.
16085575
In Commercial Distribution

  • 00887517559395 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 5.5x70mm Cann
Nuvasive, Inc.
16085570
In Commercial Distribution

  • 00887517559388 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 5.5x65mm Cann
Nuvasive, Inc.
16085565
In Commercial Distribution

  • 00887517559371 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 5.5x60mm Cann
Nuvasive, Inc.
16085560
In Commercial Distribution

  • 00887517559364 ()


  • Bone-screw internal spinal fixation system, non-sterile
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