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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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Triad CC Trial Drill Guide, 11mm 7°
Nuvasive, Inc.
1835668
In Commercial Distribution

  • 00887517817792 ()


  • Surgical implant/trial-implant/sizer holder, reusable
Triad CC Trial Drill Guide, 10mm 7°
Nuvasive, Inc.
1835667
In Commercial Distribution

  • 00887517817785 ()


  • Surgical implant/trial-implant/sizer holder, reusable
Triad CC Trial Drill Guide, 9mm 7°
Nuvasive, Inc.
1835666
In Commercial Distribution

  • 00887517817778 ()


  • Surgical implant/trial-implant/sizer holder, reusable
Triad CC Trial Drill Guide, 8mm 7°
Nuvasive, Inc.
1835665
In Commercial Distribution

  • 00887517817761 ()


  • Surgical implant/trial-implant/sizer holder, reusable
Triad CC Trial Drill Guide, 7mm 7°
Nuvasive, Inc.
1835664
In Commercial Distribution

  • 00887517817754 ()


  • Surgical implant/trial-implant/sizer holder, reusable
Triad CC Trial Drill Guide, 6mm 7°
Nuvasive, Inc.
1835663
In Commercial Distribution

  • 00887517817747 ()


  • Surgical implant/trial-implant/sizer holder, reusable
Triad CC Trial Drill Guide, 5mm 7°
Nuvasive, Inc.
1835662
In Commercial Distribution

  • 00887517817730 ()


  • Surgical implant/trial-implant/sizer holder, reusable
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
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