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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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MaXcess MAS TLIF Blade, 120mm C-C Tube
Nuvasive, Inc.
1628289
In Commercial Distribution

  • 00887517146120 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 110mm C-C Tube
Nuvasive, Inc.
1628288
In Commercial Distribution

  • 00887517146113 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 100mm C-C Tube
Nuvasive, Inc.
1628287
In Commercial Distribution

  • 00887517146106 ()


  • Surgical retraction system, reusable
ASCENT LE CC BIAS ANGLE SCREWS (66-0024)
Orthofix US LLC
450288-0001
In Commercial Distribution

  • 18257200081981 ()
66-0024

  • Bone-screw internal spinal fixation system, non-sterile
MaXcess MAS TLIF Blade, 90mm C-C Tube
Nuvasive, Inc.
1628286
In Commercial Distribution

  • 00887517145697 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 80mm C-C Tube
Nuvasive, Inc.
1628285
In Commercial Distribution

  • 00887517145680 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 70mm C-C Tube
Nuvasive, Inc.
1628284
In Commercial Distribution

  • 00887517145673 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 60mm C-C Tube
Nuvasive, Inc.
1628283
In Commercial Distribution

  • 00887517145666 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 50mm C-C Tube
Nuvasive, Inc.
1628282
In Commercial Distribution

  • 00887517145659 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 40mm C-C Tube
Nuvasive, Inc.
1628281
In Commercial Distribution

  • 00887517145642 ()


  • Surgical retraction system, reusable
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