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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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LIF Trial, 1/3 Rasped, Grooves, 10 x 22 x 70 x 10°
ALPHATEC SPINE, INC.
CI-11070-10-10227010
In Commercial Distribution

  • 00840180511244 ()


  • Spinal implant trial
LIF Trial, 1/3 Rasped, Grooves, 8 x 22 x 70 x 10°
ALPHATEC SPINE, INC.
CI-11070-10-08227010
In Commercial Distribution

  • 00840180511237 ()


  • Spinal implant trial
LIF Trial, 1/3 Rasped, Grooves, 6 x 22 x 70 x 10°
ALPHATEC SPINE, INC.
CI-11070-10-06227010
In Commercial Distribution

  • 00840180511220 ()


  • Spinal implant trial
LIF Trial, 1/3 Rasped, Grooves, 12 x 18 x 70 x 10°
ALPHATEC SPINE, INC.
CI-11070-10-12187010
In Commercial Distribution

  • 00840180511213 ()


  • Spinal implant trial
ALIF Trial Rasp Template, 4 x 34 x 24mm
ALPHATEC SPINE, INC.
CI-11003-043424
In Commercial Distribution

  • 00840180510322 ()


  • Spinal implant trial
Cervical Trial, 3 x 16 x 14, 7°
ALPHATEC SPINE, INC.
CI-11010-10-03161407
In Commercial Distribution

  • 00840180509784 ()


  • Spinal implant trial
Cervical Trial Depth Marker, 18 MM
ALPHATEC SPINE, INC.
CI-10971-08181607
In Commercial Distribution

  • 00840180508480 ()


  • Spinal implant trial
Cervical Trial Depth Marker 16 MM
ALPHATEC SPINE, INC.
CI-10971-08161407
In Commercial Distribution

  • 00840180508473 ()


  • Spinal implant trial
Cervical Trial Depth Marker 14 mm
ALPHATEC SPINE, INC.
CI-10971-08141207
In Commercial Distribution

  • 00840180508466 ()


  • Spinal implant trial
LIF Trial, Rasp, 22 MM, 10P, 10°
ALPHATEC SPINE, INC.
CI-10803-10-10227010
In Commercial Distribution

  • 00840180504826 ()


  • Spinal implant trial
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