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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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Needle Tips 20 Ga.
HENRY SCHEIN, INC.
1125979
In Commercial Distribution

  • 00304040051443 ()
  • 10304040051440 ()
1125979

  • General-purpose syringe/needle
29x39x17, 20°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-L170
In Commercial Distribution

  • B0621752L170 ()
1750-L170

  • Surgical instrument/implant depth limiter, reusable
23x29x19, 20°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-S190
In Commercial Distribution

  • B0621750S190 ()
1750-S190

  • Surgical instrument/implant depth limiter, reusable
23x29x17, 20°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-S170
In Commercial Distribution

  • B0621750S170 ()
1750-S170

  • Surgical instrument/implant depth limiter, reusable
23x29x15, 20°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-S150
In Commercial Distribution

  • B0621750S150 ()
1750-S150

  • Surgical instrument/implant depth limiter, reusable
23x29x13, 20°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-S130
In Commercial Distribution

  • B0621750S130 ()
1750-S130

  • Surgical instrument/implant depth limiter, reusable
23x29x11, 20°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-S110
In Commercial Distribution

  • B0621750S110 ()
1750-S110

  • Surgical instrument/implant depth limiter, reusable
26x35x19, 20°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-M190
In Commercial Distribution

  • B0621750M190 ()
1750-M190

  • Surgical instrument/implant depth limiter, reusable
26x35x17, 20°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-M170
In Commercial Distribution

  • B0621750M170 ()
1750-M170

  • Surgical instrument/implant depth limiter, reusable
26x35x15, 20°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-M150
In Commercial Distribution

  • B0621750M150 ()
1750-M150

  • Abdominal/ENT/orthopaedic surgical probe, reusable
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