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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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SPINAL BLOCK TRAY
DEROYAL INDUSTRIES, INC.
89-10937
In Commercial Distribution

  • 50749756380473 ()
  • 00749756380478 ()
89-10937

  • Peripheral anaesthesia single-administration set, non-medicated
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
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