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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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TLIF BULLET TRIAL L32 x W9 x A0 x H14
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489299361 ()
TI.2018

  • Bone-screw internal spinal fixation system, non-sterile
TLIF BULLET TRIAL L32 x W9 x A0 x H12
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489299347 ()
TI.2016

  • Bone-screw internal spinal fixation system, non-sterile
TLIF BULLET TRIAL L32 x W9 x A0 x H10
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489299323 ()
TI.2014

  • Bone-screw internal spinal fixation system, non-sterile
TLIF BULLET TRIAL L32 x W9 x A0 x H9
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489299316 ()
TI.2013

  • Bone-screw internal spinal fixation system, non-sterile
TLIF BULLET TRIAL L32 x W9 x A0 x H8
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489299309 ()
TI.2012

  • Bone-screw internal spinal fixation system, non-sterile
TLIF BULLET TRIAL L28 x W9 x A0 x H16
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489299286 ()
TI.2010

  • Bone-screw internal spinal fixation system, non-sterile
TLIF BULLET TRIAL L28 x W9 x A0 x H14
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489299262 ()
TI.2008

  • Bone-screw internal spinal fixation system, non-sterile
TLIF BULLET TRIAL L28 x W9 x A0 x H12
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489299248 ()
TI.2006

  • Bone-screw internal spinal fixation system, non-sterile
TLIF BULLET TRIAL L28 x W9 x A0 x H10
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489299224 ()
TI.2004

  • Bone-screw internal spinal fixation system, non-sterile
TLIF BULLET TRIAL L28 x W9 x A0 x H9
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489299217 ()
TI.2003

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