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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 L43
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039801126 ()
TP.PL.0343

  • 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 L46
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039801102 ()
TP.PL.0246

  • 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 - 2 level plate L42
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039801089 ()
TP.PL.0242

  • Spinal fixation plate, non-bioabsorbable
Fortis ACP - 2 level plate L40
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039801072 ()
TP.PL.0240

  • Spinal fixation plate, non-bioabsorbable
Fortis ACP - 2 level plate L38
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039801065 ()
TP.PL.0238

  • Spinal fixation plate, non-bioabsorbable
Fortis ACP - 2 level plate L36
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039801058 ()
TP.PL.0236

  • Spinal fixation plate, non-bioabsorbable
Fortis ACP - 2 level plate L34
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039801041 ()
TP.PL.0234

  • Spinal fixation plate, non-bioabsorbable
Fortis ACP - 2 level plate L32
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039801034 ()
TP.PL.0232

  • Spinal fixation plate, non-bioabsorbable
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