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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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Rod Pre-Bent 6.0 x 110mm
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039826389 ()
V-0202 110

  • Spinal fixation plate, non-bioabsorbable
Rod Pre-Bent 6.0 x 95mm
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039826365 ()
V-0202 095

  • Spinal fixation plate, non-bioabsorbable
Fenestrated Facet Screw Cannulated D5.5 x 60
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039825245 ()
FT.FC.5560

  • Bone-screw internal spinal fixation system, non-sterile
Fenestrated Facet Screw Cannulated D5.5 x 55
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039825238 ()
FT.FC.5555

  • Bone-screw internal spinal fixation system, non-sterile
Fenestrated Facet Screw Cannulated D5.5 x 50
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039825221 ()
FT.FC.5550

  • Bone-screw internal spinal fixation system, non-sterile
Fenestrated Facet Screw Cannulated D5.5 x 45
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039825214 ()
FT.FC.5545

  • Bone-screw internal spinal fixation system, non-sterile
Fenestrated Facet Screw Cannulated D5.5 x 40
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039825207 ()
FT.FC.5540

  • Bone-screw internal spinal fixation system, non-sterile
Fenestrated Facet Screw Cannulated D5.5 x 35
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039825191 ()
FT.FC.5535

  • Bone-screw internal spinal fixation system, non-sterile
Fenestrated Facet Screw Cannulated D5.5 x 30
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039825184 ()
FT.FC.5530

  • Bone-screw internal spinal fixation system, non-sterile
Fenestrated Facet Screw Cannulated D5.5 x 25
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039825177 ()
FT.FC.5525

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