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 L45 x W18 x A0 x H13
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489299583 ()
DI.2040

  • 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
DLIF Trial L45 x W18 x A0 x H7
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489299521 ()
DI.2034

  • Spinal implant trial
TRIAL L12 x W14 x A7 x H5
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489299392 ()
AC.2025

  • Bone-screw internal spinal fixation system, non-sterile
TLIF BULLET TRIAL L32 x W9 x A0 x H16
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489299385 ()
TI.2020

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

  • 08809489299354 ()
TI.2017

  • Bone-screw internal spinal fixation system, non-sterile
TLIF BULLET TRIAL L32 x W9 x A0 x H11
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489299330 ()
TI.2015

  • 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
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