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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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CoCr Curved Rod D5.5 x 65mm
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039817981 ()
AC.RC.5065

  • Bone-screw internal spinal fixation system, non-sterile
CoCr Curved Rod D5.5 x 60mm
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039817974 ()
AC.RC.5060

  • Bone-screw internal spinal fixation system, non-sterile
CoCr Curved Rod D5.5 x 55mm
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039817967 ()
AC.RC.5055

  • Bone-screw internal spinal fixation system, non-sterile
CoCr Curved Rod D5.5 x 50mm
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039817950 ()
AC.RC.5050

  • Bone-screw internal spinal fixation system, non-sterile
CoCr Curved Rod D5.5 x 45mm
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039817943 ()
AC.RC.5045

  • Bone-screw internal spinal fixation system, non-sterile
CoCr Curved Rod D5.5 x 40mm
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039817936 ()
AC.RC.5040

  • Bone-screw internal spinal fixation system, non-sterile
CoCr Curved Rod D5.5 x 35mm
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039817929 ()
AC.RC.5035

  • Bone-screw internal spinal fixation system, non-sterile
Transforaminal Lumbar Interbody Fusion Curved Cage L28 x W9 x H16 x A4
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039817868 ()
TCP.28090416

  • Bone-screw internal spinal fixation system, non-sterile
Rod to Rod Cross Connector. The Atoll OCT Spinal System is intended for use as an aid in spine fusion. It consists of screws, hooks, rods, and connectors. These components are available in a variety of sizes to allow for a variety of configurations to better fit each individual patient's pathology. The Atoll OCT Spinal System components are manufactured from medical implant grade titanium alloy Ti-6Al-4V (ELI) per ASTM F-136 or ISO 5832-3.
Seaspine Orthopedics Corporation
16-22-0000
In Commercial Distribution

  • 10889981033866 ()

  • N/A
16-22-0000

  • Bone-screw internal spinal fixation system connector
TLIF Implant/Trial Inserter
Seaspine Orthopedics Corporation
93-4201
In Commercial Distribution

  • 10889981030957 ()

  • N/A
93-4201

  • Orthopaedic inorganic implant inserter/extractor, reusable
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