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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Gauntlet, Large
Koya Medical, Inc.
F-0030-03
In Commercial Distribution

  • 00850012532071 ()
F-0030-03

  • Wearable sequential venous compression system
Gauntlet, X-Large
Koya Medical, Inc.
F-0030-04
In Commercial Distribution

  • 00850012532064 ()
F-0030-04

  • Wearable sequential venous compression system
Arm Liner, Large
Koya Medical, Inc.
F-0020-02
In Commercial Distribution

  • 00850012532057 ()
F-0020-02

  • Wearable sequential venous compression system
Arm Liner, Medium
Koya Medical, Inc.
F-0020-02
In Commercial Distribution

  • 00850012532040 ()
F-0020-02

  • Wearable sequential venous compression system
Arm Liner, Small
Koya Medical, Inc.
F-0020-01
In Commercial Distribution

  • 00850012532033 ()
F-0020-01

  • Wearable sequential venous compression system
Arm Garmet, Dayspring, Long
Koya Medical, Inc.
F-0010-03
In Commercial Distribution

  • 00850012532026 ()
F-0010-03

  • Wearable sequential venous compression system
Arm Garmet, Dayspring, Medium
Koya Medical, Inc.
F-0010-02
In Commercial Distribution

  • 00850012532019 ()
F-0010-02

  • Wearable sequential venous compression system
Arm Garmet, Dayspring, Short
Koya Medical, Inc.
F-0010-01
In Commercial Distribution

  • 00850012532002 ()
F-0010-01

  • Wearable sequential venous compression system
Uni-Gold™ Recombigen® HIV-1/2
TRINITY BIOTECH PUBLIC LIMITED COMPANY
1206506
Not in Commercial Distribution

  • 05391516746106 ()

  • 20 Tests
1206506

  • HIV1/HIV2 antibody IVD, kit, immunochromatographic test (ICT), rapid, professional/self-test
Wart Freezer Cryogenic Treatment 1-Step Wart Remover
MEIJER, INC.
4080389
In Commercial Distribution

  • 10713733086148 ()
  • 00713733086141 ()

  • Height: 155 Millimeter
4080389

  • Wart-removal cryogenic kit
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