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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 - 3 level plate L78
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039801232 ()
TP.PL.0378

  • Spinal fixation plate, non-bioabsorbable
Fortis ACP - 3 level plate L74
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039801225 ()
TP.PL.0374

  • Spinal fixation plate, non-bioabsorbable
Fortis ACP - 3 level plate L70
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039801218 ()
TP.PL.0370

  • Spinal fixation plate, non-bioabsorbable
Fortis ACP - 3 level plate L67
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039801201 ()
TP.PL.0367

  • Spinal fixation plate, non-bioabsorbable
Fortis ACP - 3 level plate L64
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039801195 ()
TP.PL.0364

  • Spinal fixation plate, non-bioabsorbable
Fortis ACP - 3 level plate L46
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039801133 ()
TP.PL.0346

  • Spinal fixation plate, non-bioabsorbable
Fortis ACP - 3 level plate L40
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039801119 ()
TP.PL.0340

  • Spinal fixation plate, non-bioabsorbable
Fortis ACP - 2 level plate L44
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039801096 ()
TP.PL.0244

  • Spinal fixation plate, non-bioabsorbable
Fortis ACP - 1 level plate L22
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039800969 ()
TP.PL.0122

  • Spinal fixation plate, non-bioabsorbable
Fortis ACP - 1 level plate L20
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039800952 ()
TP.PL.0120

  • Spinal fixation plate, non-bioabsorbable
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