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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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MANU-HiT AIR T
DEROYAL INDUSTRIES, INC.
SP0405-R32
In Commercial Distribution

  • 50749756380367 ()
  • 00749756380362 ()
SP0405-R32

  • Hand/finger splint, single-use
MANU-HiT AIR T
DEROYAL INDUSTRIES, INC.
SP0405-R31
In Commercial Distribution

  • 50749756380350 ()
  • 00749756380355 ()
SP0405-R31

  • Hand/finger splint, single-use
MANU-HiT AIR T
DEROYAL INDUSTRIES, INC.
SP0405-L32
In Commercial Distribution

  • 50749756380343 ()
  • 00749756380348 ()
SP0405-L32

  • Hand/finger splint, single-use
MANU-HiT AIR ROLL
DEROYAL INDUSTRIES, INC.
SP0405-L31
In Commercial Distribution

  • 50749756380336 ()
  • 00749756380331 ()
SP0405-L31

  • Hand/finger splint, single-use
MANU-HiT AIR ROLL
DEROYAL INDUSTRIES, INC.
SP0403-R31
In Commercial Distribution

  • 50749756380329 ()
  • 00749756380324 ()
SP0403-R31

  • Hand/finger splint, single-use
MANU-HiT AIR ROLL
DEROYAL INDUSTRIES, INC.
SP0403-L31
In Commercial Distribution

  • 50749756380312 ()
  • 00749756380317 ()
SP0403-L31

  • Hand/finger splint, single-use
PACEMAKER ICD PACK
DEROYAL INDUSTRIES, INC.
89-10902
In Commercial Distribution

  • 50749756380305 ()
  • 00749756380300 ()
89-10902

  • General surgical procedure kit, non-medicated, single-use
ANGIO PACK
DEROYAL INDUSTRIES, INC.
89-10901
In Commercial Distribution

  • 50749756380244 ()
  • 00749756380249 ()
89-10901

  • Angiography kit
STRETCH NET
DEROYAL INDUSTRIES, INC.
32-2186
In Commercial Distribution

  • 50749756380190 ()
  • 00749756380195 ()
32-2186

  • Skin treatment/dressing-supportive limb/finger bandage, single-use
BASIN SET
DEROYAL INDUSTRIES, INC.
89-10894
In Commercial Distribution

  • 50749756380183 ()
  • 00749756380188 ()
89-10894

  • General surgical procedure kit, non-medicated, single-use
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