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, 100mm C-C Tube
Nuvasive, Inc.
1628287
In Commercial Distribution

  • 00887517146106 ()


  • Surgical retraction system, reusable
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
MaXcess MAS TLIF Blade, 100mm Left C-C
Nuvasive, Inc.
1684307
In Commercial Distribution

  • 00887517514028 ()


  • Surgical retraction system, reusable
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
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