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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 - 00887517650122

MaXcess MAS TLIF Blade, 120mm C-C
Nuvasive, Inc.
3500109
In Commercial Distribution

  • 00887517650122 ()


  • Surgical retraction system, reusable

MaXcess - 00887517650115

MaXcess MAS TLIF Blade, 110mm C-C
Nuvasive, Inc.
3500108
In Commercial Distribution

  • 00887517650115 ()


  • Surgical retraction system, reusable

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

ARROW - 00801902010803

Intra-Aortic Balloon: 9 Fr. 50 cc
TELEFLEX INCORPORATED
IPN000261
In Commercial Distribution

  • 00801902010803 ()

  • Total Volume: 50 Milliliter
IAB-R950-U

  • Intra-aortic balloon catheter
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