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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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ARROW - 00801902136749

Intra-Aortic Balloon: 7 Fr. 30 cc
TELEFLEX INCORPORATED
IPN038076
In Commercial Distribution

  • 00801902136749 ()

  • Catheter Gauge: 7 French
IAB-S730C

  • Intra-aortic balloon catheter

ReLine - 00887517668387

RELINE 5.5/6.0mm C-C Imp. Tray
Nuvasive, Inc.
REL5560CCIMP
In Commercial Distribution

  • 00887517668387 ()


  • Device sterilization/disinfection container, reusable

MaXcess - 00887517650153

MaXcess MAS TLIF Blade, 150mm C-C
Nuvasive, Inc.
3500112
In Commercial Distribution

  • 00887517650153 ()


  • Surgical retraction system, reusable

MaXcess - 00887517650146

MaXcess MAS TLIF Blade, 140mm C-C
Nuvasive, Inc.
3500111
In Commercial Distribution

  • 00887517650146 ()


  • Surgical retraction system, reusable

MaXcess - 00887517650139

MaXcess MAS TLIF Blade, 130mm C-C
Nuvasive, Inc.
3500110
In Commercial Distribution

  • 00887517650139 ()


  • Surgical retraction system, reusable

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
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