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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TRIAL, CC FEMORAL, OPTIMIZED, SIZE 1
Exactech, Inc.
209-01-11
In Commercial Distribution

  • 10885862054616 ()

  • SIZE 1
209-01-11

  • Knee femur prosthesis trial, reusable
PRECI-POST CC REAMER D 1 P.
Alphadent NV
2954D
In Commercial Distribution

  • 04260576943255 ()

  • Outer Diameter: 0.8 Millimeter
2954D

  • Root canal post kit
PRECI-POST CC REAMER C 1 P.
Alphadent NV
2953C
In Commercial Distribution

  • 04260576943248 ()

  • Outer Diameter: 0.75 Millimeter
2953C

  • Root canal post kit
PRECI-POST CC REAMER B 1 P.
Alphadent NV
2952B
In Commercial Distribution

  • 04260576943231 ()

  • Outer Diameter: 0.7 Millimeter
2952B

  • Root canal post kit
PRECI-POST CC REAMER A 1 P.
Alphadent NV
2951A
In Commercial Distribution

  • 04260576943224 ()

  • Outer Diameter: 0.65 Millimeter
2951A

  • Root canal post kit
MaXcess MAS TLIF Blade, 150mm C-C
Nuvasive, Inc.
3500112
In Commercial Distribution

  • 00887517650153 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 140mm C-C
Nuvasive, Inc.
3500111
In Commercial Distribution

  • 00887517650146 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 130mm C-C
Nuvasive, Inc.
3500110
In Commercial Distribution

  • 00887517650139 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 120mm C-C
Nuvasive, Inc.
3500109
In Commercial Distribution

  • 00887517650122 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 110mm C-C
Nuvasive, Inc.
3500108
In Commercial Distribution

  • 00887517650115 ()


  • Surgical retraction system, reusable
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