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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M Grey-Blue
Darco (Europe) GmbH
RIW2W-2
In Commercial Distribution

  • 24251853900300 ()
  • 04251853900306 ()
  • 14251853900303 ()
RIW2W-2

  • Ankle/foot orthosis
S Grey-Blue
Darco (Europe) GmbH
RIW2W-1
In Commercial Distribution

  • 24251853900294 ()
  • 04251853900290 ()
  • 14251853900297 ()
RIW2W-1

  • Ankle/foot orthosis
XS Grey-Blue
Darco (Europe) GmbH
RIW2W-0
In Commercial Distribution

  • 14251853900280 ()
  • 04251853900283 ()
  • 24251853900287 ()
RIW2W-0

  • Ankle/foot orthosis
XL Grey-Blue
Darco (Europe) GmbH
RIW2-4
In Commercial Distribution

  • 14251853900273 ()
  • 04251853900276 ()
  • 24251853900270 ()
RIW2-4

  • Ankle/foot orthosis
L Grey-Blue
Darco (Europe) GmbH
RIW2-3
In Commercial Distribution

  • 14251853900266 ()
  • 04251853900269 ()
  • 24251853900263 ()
RIW2-3

  • Ankle/foot orthosis
M Grey-Blue
Darco (Europe) GmbH
RIW2-2
In Commercial Distribution

  • 24251853900256 ()
  • 04251853900252 ()
  • 14251853900259 ()
RIW2-2

  • Ankle/foot orthosis
S Grey-Blue
Darco (Europe) GmbH
RIW2-1
In Commercial Distribution

  • 24251853900249 ()
  • 04251853900245 ()
  • 14251853900242 ()
RIW2-1

  • Ankle/foot orthosis
XS Grey-Blue
Darco (Europe) GmbH
RIW2-0
In Commercial Distribution

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

  • Ankle/foot orthosis
XL Grey
Darco (Europe) GmbH
RIW1C-4
In Commercial Distribution

  • 24251853900201 ()
  • 04251853900207 ()
  • 14251853900204 ()
RIW1C-4

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

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

  • Ankle/foot orthosis
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