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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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7 In WRIST SPLINT
DEROYAL INDUSTRIES, INC.
5067-01
In Commercial Distribution

  • 00749756670227 ()
5067-01

  • Hand/finger splint, single-use
24 In Knee Immobilizer
DEROYAL INDUSTRIES, INC.
V4433-24
In Commercial Distribution

  • 00749756162678 ()
V4433-24

  • Knee immobilizer
22 In Knee Immobilizer
DEROYAL INDUSTRIES, INC.
V4433-22
In Commercial Distribution

  • 00749756162661 ()
V4433-22

  • Knee immobilizer
16 In Knee Immobilizer
DEROYAL INDUSTRIES, INC.
V1160917
In Commercial Distribution

  • 00749756162593 ()
V1160917

  • Knee immobilizer
WRIST SPLINT, 8 In
DEROYAL INDUSTRIES, INC.
23-325A-05-POC
In Commercial Distribution

  • 00749756932356 ()
23-325A-05-POC

  • Hand/finger splint, single-use
WRIST SPLINT, 8 In
DEROYAL INDUSTRIES, INC.
23-325A-04-POC
In Commercial Distribution

  • 00749756932349 ()
23-325A-04-POC

  • Hand/finger splint, single-use
WRIST SPLINT, 8 In
DEROYAL INDUSTRIES, INC.
23-325A-03-POC
In Commercial Distribution

  • 00749756932332 ()
23-325A-03-POC

  • Hand/finger splint, single-use
WRIST SPLINT, 8 In
DEROYAL INDUSTRIES, INC.
23-325A-02-POC
In Commercial Distribution

  • 00749756932325 ()
23-325A-02-POC

  • Hand/finger splint, single-use
WRIST SPLINT, 8 In
DEROYAL INDUSTRIES, INC.
23-325A-01-POC
In Commercial Distribution

  • 00749756932318 ()
23-325A-01-POC

  • Hand/finger splint, single-use
1 In AORTIC GAUZE
DEROYAL INDUSTRIES, INC.
32-2079
In Commercial Distribution

  • 50749756894017 ()
  • 00749756894012 ()
32-2079

  • Wound-nonadherent dressing, permeable, non-antimicrobial
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