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
Nuvasive, Inc.
3500107
In Commercial Distribution

  • 00887517650108 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 90mm C-C
Nuvasive, Inc.
3500106
In Commercial Distribution

  • 00887517650092 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 80mm C-C
Nuvasive, Inc.
3500105
In Commercial Distribution

  • 00887517650085 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 70mm C-C
Nuvasive, Inc.
3500104
In Commercial Distribution

  • 00887517650078 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 60mm C-C
Nuvasive, Inc.
3500103
In Commercial Distribution

  • 00887517650061 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 50mm C-C
Nuvasive, Inc.
3500102
In Commercial Distribution

  • 00887517650054 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 40mm C-C
Nuvasive, Inc.
3500101
In Commercial Distribution

  • 00887517650047 ()


  • Surgical retraction system, reusable
DIAMOND 3.0 ANG CC SHRP SIDE
Bausch & Lomb Incorporated
E0104 ACC3.0
In Commercial Distribution

  • 00757770440290 ()
E0104 ACC3.0

  • Ophthalmic knife, reusable
DIAMOND 2.5 ANG CC SHRP SIDE
Bausch & Lomb Incorporated
E0104 ACC2.5
In Commercial Distribution

  • 00757770440276 ()
E0104 ACC2.5

  • Ophthalmic knife, reusable
MaXcess-C Blade, 30mm C-C Smooth Right
Nuvasive, Inc.
7991713
In Commercial Distribution

  • 00887517201201 ()


  • Surgical retraction system, reusable
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