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 Type Device Class Implantable

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GRID IRON® XR ROM
DEROYAL INDUSTRIES, INC.
1-519A-02
In Commercial Distribution

  • 00749756846264 ()
1-519A-02

  • Ankle/foot orthosis
GRID IRON® XR
DEROYAL INDUSTRIES, INC.
1-518A-05
In Commercial Distribution

  • 00749756838740 ()
1-518A-05

  • Ankle/foot orthosis
GRID IRON® XR
DEROYAL INDUSTRIES, INC.
1-518A-04
In Commercial Distribution

  • 00749756838733 ()
1-518A-04

  • Ankle/foot orthosis
GRID IRON® XR
DEROYAL INDUSTRIES, INC.
1-518A-03
In Commercial Distribution

  • 00749756838726 ()
1-518A-03

  • Ankle/foot orthosis
GRID IRON® XR
DEROYAL INDUSTRIES, INC.
1-518A-02
In Commercial Distribution

  • 00749756838719 ()
1-518A-02

  • Ankle/foot orthosis
GRID IRON® XR
DEROYAL INDUSTRIES, INC.
1-518A-01
In Commercial Distribution

  • 00749756838702 ()
1-518A-01

  • Ankle/foot orthosis
PACESETTER® WALKER
DEROYAL INDUSTRIES, INC.
1-513A-05
In Commercial Distribution

  • 00749756834094 ()
1-513A-05

  • Ankle/foot orthosis
PACESETTER® WALKER
DEROYAL INDUSTRIES, INC.
1-513A-04
In Commercial Distribution

  • 00749756834087 ()
1-513A-04

  • Ankle/foot orthosis
PACESETTER® WALKER
DEROYAL INDUSTRIES, INC.
1-513A-03
In Commercial Distribution

  • 00749756834070 ()
1-513A-03

  • Ankle/foot orthosis
PACESETTER® WALKER
DEROYAL INDUSTRIES, INC.
1-513A-02
In Commercial Distribution

  • 00749756834063 ()
1-513A-02

  • Ankle/foot orthosis
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