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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, 90mm Left C-C
Nuvasive, Inc.
1684306
In Commercial Distribution

  • 00887517514011 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 80mm Left C-C
Nuvasive, Inc.
1684305
In Commercial Distribution

  • 00887517514004 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 70mm Left C-C
Nuvasive, Inc.
1684304
In Commercial Distribution

  • 00887517499592 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 60mm Left C-C
Nuvasive, Inc.
1684303
In Commercial Distribution

  • 00887517499585 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 50mm Left C-C
Nuvasive, Inc.
1684302
In Commercial Distribution

  • 00887517499578 ()


  • Surgical retraction system, reusable
Triad CC Trial Drill Guide, 11mm 7°
Nuvasive, Inc.
1835668
In Commercial Distribution

  • 00887517817792 ()


  • Surgical implant/trial-implant/sizer holder, reusable
MaXcess MAS TLIF Blade, 100mm Right C-C
Nuvasive, Inc.
1685307
In Commercial Distribution

  • 00887517614469 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 90mm Right C-C
Nuvasive, Inc.
1685306
In Commercial Distribution

  • 00887517614452 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 70mm Right C-C
Nuvasive, Inc.
1685304
In Commercial Distribution

  • 00887517614438 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 80mm Right C-C
Nuvasive, Inc.
1685305
In Commercial Distribution

  • 00887517614445 ()


  • Surgical retraction system, reusable
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