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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 Class Implantable

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SpheRx - 00887517108524

SpheRx PPS Base, Ins /Imp Tray
Nuvasive, Inc.
7770050
In Commercial Distribution

  • 00887517108524 ()


  • Device sterilization/disinfection container, reusable

Bendini - 00887517107787

Bendini Swivel Pointer
Nuvasive, Inc.
8210300
In Commercial Distribution

  • 00887517107787 ()


  • Spinal rod bending system

MaXcess - 00887517107329

MAS TLIF Ambiblade, 110mm Alpha
Nuvasive, Inc.
1577211
In Commercial Distribution

  • 00887517107329 ()


  • Surgical retraction system, reusable

MaXcess - 00887517107312

MAS TLIF Ambiblade, 90mm Alpha
Nuvasive, Inc.
1577209
In Commercial Distribution

  • 00887517107312 ()


  • Surgical retraction system, reusable

MaXcess - 00887517107305

Self Retaining Light Cable
Nuvasive, Inc.
1577130
In Commercial Distribution

  • 00887517107305 ()


  • Fibreoptic light cable

MaXcess - 00887517106834

MaXcess-C Blade, 19x70mm 3-Tooth
Nuvasive, Inc.
1576065
In Commercial Distribution

  • 00887517106834 ()


  • Surgical retraction system, reusable

MaXcess - 00887517106827

MaXcess-C Blade, 19x30mm 3-Tooth
Nuvasive, Inc.
1576061
In Commercial Distribution

  • 00887517106827 ()


  • Surgical retraction system, reusable

MaXcess - 00887517106810

MaXcess-C Blade, 19x60mm Blunt
Nuvasive, Inc.
1576054
In Commercial Distribution

  • 00887517106810 ()


  • Surgical retraction system, reusable

MaXcess - 00887517106803

MaXcess-C Blade, 19x40mm Serrated
Nuvasive, Inc.
1576042
In Commercial Distribution

  • 00887517106803 ()


  • Surgical retraction system, reusable

MaXcess - 00887517106391

MaXcess-C Blade, 14x60mm Blunt
Nuvasive, Inc.
1576034
In Commercial Distribution

  • 00887517106391 ()


  • Surgical retraction system, reusable
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