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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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Fortis ACP - 4 level plate L92
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039801348 ()
TP.PL.0492

  • Spinal fixation plate, non-bioabsorbable
Fortis ACP - 4 level plate L88
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039801331 ()
TP.PL.0488

  • Spinal fixation plate, non-bioabsorbable
Fortis ACP - 4 level plate L84
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039801324 ()
TP.PL.0484

  • Spinal fixation plate, non-bioabsorbable
Fortis ACP - 4 level plate L80
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039801317 ()
TP.PL.0480

  • Spinal fixation plate, non-bioabsorbable
Fortis ACP - 4 level plate L76
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039801300 ()
TP.PL.0476

  • Spinal fixation plate, non-bioabsorbable
Fortis ACP - 4 level plate L72
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039801294 ()
TP.PL.0472

  • Spinal fixation plate, non-bioabsorbable
Fortis ACP - 4 level plate L68
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039801287 ()
TP.PL.0468

  • Spinal fixation plate, non-bioabsorbable
Fortis ACP - 4 level plate L64
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039801270 ()
TP.PL.0464

  • Spinal fixation plate, non-bioabsorbable
Fortis ACP - 4 level plate L60
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039801263 ()
TP.PL.0460

  • Spinal fixation plate, non-bioabsorbable
Fortis ACP - 4 level plate L56
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039801256 ()
TP.PL.0456

  • Spinal fixation plate, non-bioabsorbable
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