SEARCH RESULTS FOR: (*Fake Texas A*)(34858 results)

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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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Double Ended Trial/Rasp with Stop Instrument
ALLIANCE PARTNERS LLC
1412T-210-S
In Commercial Distribution

  • M6861412T210S0 ()

  • Trial/Rasp Size: 14x12x7mm x 0° (W x L x H)
1412T-210-S

  • Spinal implant trial
  • Bone file/rasp, manual, reusable
Double Ended Trial/Rasp Instrument
ALLIANCE PARTNERS LLC
1412T-210
In Commercial Distribution

  • M6861412T2100 ()

  • Trial/Rasp Size: 14x12x7mm x 0° (W x L x H)
1412T-210

  • Bone file/rasp, manual, reusable
  • Spinal implant trial
TLIF(B) Caddy Case L32 x W9
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557207915 ()
TI.3302

  • Spinal implant trial
TLIF(B) Caddy Case L28 x W9
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557207908 ()
TI.3301

  • Spinal implant trial
TLIF(B) Trial L40 x W11 x H16
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557207106 ()
TI.2150

  • Spinal implant trial
TLIF(B) Trial L40 x W11 x H14
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557207083 ()
TI.2148

  • Spinal implant trial
TLIF(B) Trial L40 x W9 x H7
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557206819 ()
TI.2121

  • Spinal implant trial
TLIF(B) Trial L38 x W11 x H16
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557206802 ()
TI.2120

  • Spinal implant trial
TLIF(B) Trial L38 x W11 x H15
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557206796 ()
TI.2119

  • Spinal implant trial
TLIF(B) Trial L38 x W11 x H14
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557206789 ()
TI.2118

  • Spinal implant trial
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