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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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TRIAL L12 x W14 x H8
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489298975 ()
AC.2020

  • Bone-screw internal spinal fixation system, non-sterile
TRIAL L12 x W14 x H5
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489298951 ()
AC.2017

  • Bone-screw internal spinal fixation system, non-sterile
TRIAL L14 x W16 x H8
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489298890 ()
AC.2036

  • Bone-screw internal spinal fixation system, non-sterile
TRIAL L12 x W14 x H6
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489298869 ()
AC.2018

  • Bone-screw internal spinal fixation system, non-sterile
PLIF PADDLE DISTRACTOR (H17)
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489298852 ()
PI.2211

  • Bone-screw internal spinal fixation system, non-sterile
PLIF PADDLE DISTRACTOR (H16)
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489298845 ()
PI.2210

  • Bone-screw internal spinal fixation system, non-sterile
PLIF PADDLE DISTRACTOR (H15)
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489298838 ()
PI.2209

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

  • 08809489298814 ()
PI.2207

  • Bone-screw internal spinal fixation system, non-sterile
PLIF PADDLE DISTRACTOR (H11)
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489298791 ()
PI.2205

  • Bone-screw internal spinal fixation system, non-sterile
PLIF PADDLE DISTRACTOR (H9)
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489298777 ()
PI.2203

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