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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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PLIF TRIAL L26 x A0 x H10
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489298708 ()
PI.2070

  • Bone-screw internal spinal fixation system, non-sterile
PLIF TRIAL L26 x A0 x H9
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489298692 ()
PI.2069

  • Bone-screw internal spinal fixation system, non-sterile
PLIF TRIAL L26 x A0 x H8
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489298685 ()
PI.2068

  • Bone-screw internal spinal fixation system, non-sterile
PLIF TRIAL L26 x A8 x H14
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489298678 ()
PI.2096

  • Bone-screw internal spinal fixation system, non-sterile
PLIF TRIAL L26 x A8 x H13
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489298661 ()
PI.2095

  • Bone-screw internal spinal fixation system, non-sterile
PLIF TRIAL L26 x A8 x H12
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489298654 ()
PI.2094

  • Bone-screw internal spinal fixation system, non-sterile
PLIF TRIAL L26 x A8 x H11
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489298647 ()
PI.2093

  • Bone-screw internal spinal fixation system, non-sterile
PLIF TRIAL L26 x A8 x H10
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489298630 ()
PI.2092

  • Bone-screw internal spinal fixation system, non-sterile
PLIF TRIAL L26 x A8 x H9
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489298623 ()
PI.2091

  • Bone-screw internal spinal fixation system, non-sterile
PLIF TRIAL L26 x A8 x H8
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489298616 ()
PI.2090

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