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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CC CEMENTED FEM TRIAL, SZ 2 THREADED
Exactech, Inc.
209-02-02
In Commercial Distribution

  • 10885862054678 ()

  • SIZE 2
209-02-02

  • Knee femur prosthesis trial, reusable
CC CEMENTED FEM TRIAL, SZ 1, THREADED
Exactech, Inc.
209-02-01
In Commercial Distribution

  • 10885862054661 ()

  • SIZE 1
209-02-01

  • Knee femur prosthesis trial, reusable
MaXcess MAS TLIF Blade, 100mm Right C-C
Nuvasive, Inc.
1685307
In Commercial Distribution

  • 00887517614469 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 90mm Right C-C
Nuvasive, Inc.
1685306
In Commercial Distribution

  • 00887517614452 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 80mm Right C-C
Nuvasive, Inc.
1685305
In Commercial Distribution

  • 00887517614445 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 70mm Right C-C
Nuvasive, Inc.
1685304
In Commercial Distribution

  • 00887517614438 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 60mm Right C-C
Nuvasive, Inc.
1685303
In Commercial Distribution

  • 00887517614421 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 50mm Right C-C
Nuvasive, Inc.
1685302
In Commercial Distribution

  • 00887517614414 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 100mm Left C-C
Nuvasive, Inc.
1684307
In Commercial Distribution

  • 00887517514028 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 90mm Left C-C
Nuvasive, Inc.
1684306
In Commercial Distribution

  • 00887517514011 ()


  • Surgical retraction system, reusable
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