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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 - 00887517650108

MaXcess MAS TLIF Blade, 100mm C-C
Nuvasive, Inc.
3500107
In Commercial Distribution

  • 00887517650108 ()


  • Surgical retraction system, reusable

MaXcess - 00887517650092

MaXcess MAS TLIF Blade, 90mm C-C
Nuvasive, Inc.
3500106
In Commercial Distribution

  • 00887517650092 ()


  • Surgical retraction system, reusable

MaXcess - 00887517650085

MaXcess MAS TLIF Blade, 80mm C-C
Nuvasive, Inc.
3500105
In Commercial Distribution

  • 00887517650085 ()


  • Surgical retraction system, reusable

MaXcess - 00887517650078

MaXcess MAS TLIF Blade, 70mm C-C
Nuvasive, Inc.
3500104
In Commercial Distribution

  • 00887517650078 ()


  • Surgical retraction system, reusable

MaXcess - 00887517650061

MaXcess MAS TLIF Blade, 60mm C-C
Nuvasive, Inc.
3500103
In Commercial Distribution

  • 00887517650061 ()


  • Surgical retraction system, reusable

MaXcess - 00887517650054

MaXcess MAS TLIF Blade, 50mm C-C
Nuvasive, Inc.
3500102
In Commercial Distribution

  • 00887517650054 ()


  • Surgical retraction system, reusable

MaXcess - 00887517650047

MaXcess MAS TLIF Blade, 40mm C-C
Nuvasive, Inc.
3500101
In Commercial Distribution

  • 00887517650047 ()


  • Surgical retraction system, reusable

Bausch + Lomb - 00757770440290

DIAMOND 3.0 ANG CC SHRP SIDE
Bausch & Lomb Incorporated
E0104 ACC3.0
In Commercial Distribution

  • 00757770440290 ()
E0104 ACC3.0

  • Ophthalmic knife, reusable

Bausch + Lomb - 00757770440276

DIAMOND 2.5 ANG CC SHRP SIDE
Bausch & Lomb Incorporated
E0104 ACC2.5
In Commercial Distribution

  • 00757770440276 ()
E0104 ACC2.5

  • Ophthalmic knife, reusable

MaXcess - 00887517201201

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

  • 00887517201201 ()


  • Surgical retraction system, reusable
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