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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Darco (Europe) GmbH
RIW2-0
In Commercial Distribution

  • 24251853900232 ()
  • 04251853900238 ()
  • 14251853900235 ()
RIW2-0

  • Ankle/foot orthosis
L Grey
Darco (Europe) GmbH
RIW1C-3
In Commercial Distribution

  • 14251853900198 ()
  • 04251853900191 ()
  • 24251853900195 ()
RIW1C-3

  • Ankle/foot orthosis
NIGHT SPLINT, DORSAL LG/XLG
DJO, LLC
155-14040L-XL
In Commercial Distribution

  • 00190446683407 ()


  • Ankle/foot orthosis
NIGHT SPLINT, DORSAL SM/MED
DJO, LLC
155-14040S-M
In Commercial Distribution

  • 00190446683414 ()


  • Ankle/foot orthosis
NIGHT SPLINT, PLANTAR FASCIITIS NIGHT LG
DJO, LLC
155-79-97757
In Commercial Distribution

  • 00190446662778 ()


  • Ankle/foot orthosis
NIGHT SPLINT, PLANTAR FASCIITIS NIGHT MED
DJO, LLC
155-79-97755
In Commercial Distribution

  • 00190446662761 ()


  • Ankle/foot orthosis
NIGHT SPLINT, PLANTAR FASCIITIS NIGHT SM
DJO, LLC
155-79-97753
In Commercial Distribution

  • 00190446662754 ()


  • Ankle/foot orthosis
DJA PLANTAR FASCIITIS NIGHT SPLINT, BLACK, LARGE/XLARGE
DJO, LLC
DA161FB01-BLK-L,XL
In Commercial Distribution

  • 00190446339465 ()


  • Ankle/foot orthosis
Plantar Fasciitis Kit
BROWNMED, INC.
53105
In Commercial Distribution

  • 00082161531050 ()


  • Ankle/foot orthosis
Plantar Fasciitis Kit
BROWNMED, INC.
53104
In Commercial Distribution

  • 00082161531043 ()


  • Ankle/foot orthosis
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