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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MANU-HiT Digitus Pollex
DEROYAL INDUSTRIES, INC.
SP0326-R6
In Commercial Distribution

  • 50749756380466 ()
  • 00749756380461 ()
SP0326-R6

  • Hand/finger splint, single-use
MANU-HiT Digitus Pollex
DEROYAL INDUSTRIES, INC.
SP0326-R5
In Commercial Distribution

  • 50749756380459 ()
  • 00749756380454 ()
SP0326-R5

  • Hand/finger splint, single-use
MANU-HiT Digitus Pollex
DEROYAL INDUSTRIES, INC.
SP0326-R4
In Commercial Distribution

  • 50749756380442 ()
  • 00749756380447 ()
SP0326-R4

  • Hand/finger splint, single-use
MANU-HiT Digitus Pollex
DEROYAL INDUSTRIES, INC.
SP0326-L6
In Commercial Distribution

  • 50749756380435 ()
  • 00749756380430 ()
SP0326-L6

  • Hand/finger splint, single-use
MANU-HiT Digitus Pollex
DEROYAL INDUSTRIES, INC.
SP0326-L5
In Commercial Distribution

  • 50749756380428 ()
  • 00749756380423 ()
SP0326-L5

  • Hand/finger splint, single-use
MANU-HiT Digitus Pollex
DEROYAL INDUSTRIES, INC.
SP0326-L4
In Commercial Distribution

  • 50749756380411 ()
  • 00749756380416 ()
SP0326-L4

  • Hand/finger splint, single-use
MANU-HiT AIR
DEROYAL INDUSTRIES, INC.
SP0413-R32
In Commercial Distribution

  • 50749756380404 ()
  • 00749756380409 ()
SP0413-R32

  • Hand/finger splint, single-use
MANU-HiT AIR
DEROYAL INDUSTRIES, INC.
SP0413-R31
In Commercial Distribution

  • 50749756380398 ()
  • 00749756380393 ()
SP0413-R31

  • Hand/finger splint, single-use
MANU-HiT AIR
DEROYAL INDUSTRIES, INC.
SP0413-L32
In Commercial Distribution

  • 50749756380381 ()
  • 00749756380386 ()
SP0413-L32

  • Hand/finger splint, single-use
MANU-HiT AIR
DEROYAL INDUSTRIES, INC.
SP0413-L31
In Commercial Distribution

  • 50749756380374 ()
  • 00749756380379 ()
SP0413-L31

  • Hand/finger splint, single-use
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