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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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DLIF Trial L50 x W18 x A0 x H15
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489299712 ()
DI.2075

  • Spinal implant trial
DLIF Trial L50 x W18 x A0 x H11
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489299675 ()
DI.2071

  • Spinal implant trial
DLIF Trial L50 x W18 x A0 x H9
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489299651 ()
DI.2069

  • Spinal implant trial
DLIF Trial L50 x W18 x A0 x H7
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489299637 ()
DI.2067

  • Spinal implant trial
DLIF Trial L45 x W18 x A0 x H17
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489299620 ()
DI.2044

  • Spinal implant trial
DLIF Trial L45 x W18 x A0 x H15
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489299606 ()
DI.2042

  • Spinal implant trial
DLIF Trial L45 x W18 x A0 x H11
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489299569 ()
DI.2038

  • Spinal implant trial
DLIF Trial L45 x W18 x A0 x H9
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489299545 ()
DI.2036

  • Spinal implant trial
TLIF BULLET TRIAL L32 x W9 x A0 x H15
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489299378 ()
TI.2019

  • Bone-screw internal spinal fixation system, non-sterile
TLIF BULLET TRIAL L32 x W9 x A0 x H13
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489299354 ()
TI.2017

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