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

Show Filters

Bracket with Tube Guide
WESTMED, INC.
WP-7704
In Commercial Distribution

  • 10709078013574 ()
  • 00709078013560 ()


  • PEEP valve, single-use
No Description
Biomet Orthopedics, LLC
402439
In Commercial Distribution

  • 00880304476783 ()
402439

  • Orthopaedic cement, antimicrobial
The Perfusion Clamp is used for explanted organ recovered with aortic patch. It is a sterile, disposable and single-use device.
INSTITUT GEORGES LOPEZ
PC1025A
In Commercial Distribution

  • 23700911900949 ()
  • 13700911900942 ()
  • 53700911900940 ()
  • 33700911900946 ()


  • Kidney donor-organ preservation/transport perfusion set
The Perfusion Clamp is used for explanted organ recovered with aortic patch. It is a sterile, disposable and single-use device.
INSTITUT GEORGES LOPEZ
PC715A
In Commercial Distribution

  • 23700911900932 ()
  • 13700911900935 ()
  • 53700911900933 ()
  • 33700911900939 ()


  • Kidney donor-organ preservation/transport perfusion set
The Perfusion Clamp is used for explanted organ recovered with aortic patch. It is a sterile, disposable and single-use device.
INSTITUT GEORGES LOPEZ
PC1020A
In Commercial Distribution

  • 23700911900925 ()
  • 13700911900928 ()
  • 53700911900926 ()
  • 33700911900922 ()


  • Kidney donor-organ preservation/transport perfusion set
No Description
Biomet Orthopedics, LLC
903719
In Commercial Distribution

  • 00880304405035 ()
903719

  • Bone file/rasp, manual, reusable
No Description
Biomet Orthopedics, LLC
471782
In Commercial Distribution

  • 00880304384514 ()
471782

  • Bone-resection orthopaedic reamer, reusable
No Description
Double Medical Technology Inc.
110071900
In Commercial Distribution

  • 06902139110985 ()
110071900

  • Surgical implant handling forceps
No Description
Double Medical Technology Inc.
110041900
In Commercial Distribution

  • 06902139110664 ()
110041900

  • Surgical implant handling forceps
No Description
Double Medical Technology Inc.
110041400
In Commercial Distribution

  • 06902139110596 ()
110041400

  • Surgical drill guide, reusable
No Description
Double Medical Technology Inc.
111190600
In Commercial Distribution

  • 06902139111982 ()
111190600

  • Surgical drill guide, reusable
Non-Rebreather Mask with GSL, filter and adapter
WESTMED, INC.
0364
Not in Commercial Distribution

  • 00709078004469 ()


  • Heat/moisture exchanger/microbial medical gas filter
  • Non-rebreathing oxygen face mask
No Description
Biomet Orthopedics, LLC
402283
In Commercial Distribution

  • 00880304560796 ()
402283

  • Orthopaedic cement, antimicrobial
No Description
DERMARITE INDUSTRIES LLC
32670
In Commercial Distribution

  • 00714196391803 ()


  • Exudate-absorbent dressing, non-gel, non-antimicrobial
No Description
DERMARITE INDUSTRIES LLC
00229E
In Commercial Distribution

  • 00714196391780 ()


  • Exudate-absorbent dressing, non-gel, non-antimicrobial
No Description
DERMARITE INDUSTRIES LLC
00306E
In Commercial Distribution

  • 00714196391766 ()


  • Exudate-absorbent dressing, non-gel, non-antimicrobial
No Description
DERMARITE INDUSTRIES LLC
00259E
In Commercial Distribution

  • 00714196391742 ()


  • Exudate-absorbent dressing, non-gel, non-antimicrobial
No Description
DERMARITE INDUSTRIES LLC
32670
In Commercial Distribution

  • 00714196326706 ()
  • 01714196326705 ()


  • Exudate-absorbent dressing, non-gel, non-antimicrobial
No Description
DERMARITE INDUSTRIES LLC
00306E
In Commercial Distribution

  • 00714196306661 ()
  • 00171419630666 ()


  • Exudate-absorbent dressing, non-gel, non-antimicrobial
No Description
CHARMANT INC.
37-0075
In Commercial Distribution

  • 00883475953718 ()


  • Ophthalmic surgical device handling forceps, reusable
No Description
CHARMANT INC.
37-0064
In Commercial Distribution

  • 00883475952988 ()


  • Corneal marker, reusable
No Description
CHARMANT INC.
37-0063
In Commercial Distribution

  • 00883475952957 ()


  • Eyelid speculum, reusable
No Description
CHARMANT INC.
37-0060
In Commercial Distribution

  • 00883475952285 ()


  • Ophthalmic surgical device handling forceps, reusable
No Description
CHARMANT INC.
37-0010
In Commercial Distribution

  • 00883475651386 ()


  • Eyelid speculum, reusable
A non-sterile substance intended to be applied to exposed dentine (resulting from enamel erosion, breakage, or gingival recession) to treat dental hypersensitivity caused by physical, chemical, and physiological agents (e.g., cold, heat, contact, acid, bruxism) by forming a barrier within the dentine tubules. It is a mixture of synthetic and/or plant-derived ingredients in fluid form (e.g., gel, mouth-rinse resin, varnish); it may also have antimicrobial properties or contain fluoride for caries prevention. It is normally available [non-prescription] over-the-counter (OTC) for use in the home or healthcare facility. After application, this device cannot be reused.
AMERICAN DENTAL PRODUCTS INC
10 ml
Not in Commercial Distribution

  • 00865849000242 ()

  • Total Volume: 10 Milliliter
9515140

  • Dental coating, tooth-desensitizing
A non-sterile substance intended to be applied to exposed dentine (resulting from enamel erosion, breakage, or gingival recession) to treat dental hypersensitivity caused by physical, chemical, and physiological agents (e.g., cold, heat, contact, acid, bruxism) by forming a barrier within the dentine tubules. It is a mixture of synthetic and/or plant-derived ingredients in fluid form (e.g., gel, mouth-rinse resin, varnish); it may also have antimicrobial properties or contain fluoride for caries prevention. It is normally available [non-prescription] over-the-counter (OTC) for use in the home or healthcare facility. After application, this device cannot be reused.
AMERICAN DENTAL PRODUCTS INC
10 ml
Not in Commercial Distribution

  • 00865849000228 ()

  • Total Volume: 10 Milliliter
9515140

  • Dental coating, tooth-desensitizing
A non-sterile substance intended to be applied to exposed dentine (resulting from enamel erosion, breakage, or gingival recession) to treat dental hypersensitivity caused by physical, chemical, and physiological agents (e.g., cold, heat, contact, acid, bruxism) by forming a barrier within the dentine tubules. It is a mixture of synthetic and/or plant-derived ingredients in fluid form (e.g., gel, mouth-rinse resin, varnish); it may also have antimicrobial properties or contain fluoride for caries prevention. It is normally available [non-prescription] over-the-counter (OTC) for use in the home or healthcare facility. After application, this device cannot be reused.
AMERICAN DENTAL PRODUCTS INC
DDS
Not in Commercial Distribution

  • 00865849000204 ()


  • Dental coating, tooth-desensitizing
InspiraChamber Anti-Static Valved Holding Chamber with InspiraMask- Hospital Unit
INSPIRX, INC
IC-IML-0
In Commercial Distribution

  • 00852367007013 ()
  • 10852367007010 ()


  • Medicine chamber spacer, reusable
FlexGuide ULTRA set with Fleguide Handpiece and Tray
OMNIGUIDE, INC.
FLEX-ULTRA SET
In Commercial Distribution

  • 00852306007302 ()
FLEX-ULTRA SET

  • Urogenital surgical laser system beam guide, reusable
blue vinyl, 22mm OD, 50/bx
Vacumed
1007-MP
In Commercial Distribution

  • 00850644007589 ()
  • 08506440075896 ()
1007-MP

  • Breathing mouthpiece, single-use
The SuperPole F.R.S. (floor receptacle system) with SuperBar is a high quality, commercial grade pivoting and locking horizontal bar that connects to the SuperPole F.R.S. (a support pole that interfaces with and is supported by a receptacle that is permanently embedded into a structural concrete floor). The horizontal bar can be lifted, pivoted, and lowered to the next locking position around the F.R.S. pole. The SuperBar is intended for moderate vertical and horizontal load bearing to provide sitting and standing support for people with reduced mobility. The SuperBar is installed onto the SuperPole F.R.S. by securing a castellated collar to the pole with 3 cone point set screws. The set screws pierce into the pole and lock the collar in place, and the spring ring is used to prevent the set screws from back-threading. The castellated collar has 8 grooves strong enough for the SuperBar to support the user. When the SuperPole F.R.S. is removed from the concrete receptacle, the receptacle must be covered with a floor flush cap to provide a water-tight seal. The maximum user weight for this product is 450lbs / 205kgs. Product is not intended to support full body weight.
Healthcraft Products Inc.
FRS-SPB
In Commercial Distribution

  • 00689281035866 ()
03596

  • Hand rail
No Description
Terumo Cardiovascular Systems Corporation
45053
In Commercial Distribution

  • 50699753450535 ()
  • 00699753450530 ()


  • Cardiopulmonary bypass system blood tubing set
No Description
Terumo Cardiovascular Systems Corporation
45052
In Commercial Distribution

  • 50699753450528 ()
  • 00699753450523 ()


  • Cardiopulmonary bypass system blood tubing set
No Description
Terumo Cardiovascular Systems Corporation
45051
In Commercial Distribution

  • 50699753450511 ()
  • 00699753450516 ()


  • Cardiopulmonary bypass system blood tubing set
No Description
Terumo Cardiovascular Systems Corporation
45050
In Commercial Distribution

  • 50699753450504 ()
  • 00699753450509 ()


  • Cardiopulmonary bypass system blood tubing set
No Description
Biomet Orthopedics, LLC
110005089
In Commercial Distribution

  • 00880304567641 ()
110005089

  • Ligament bone anchor
No Description
Biomet Orthopedics, LLC
110005087
In Commercial Distribution

  • 00880304567634 ()
110005087

  • Tendon/ligament bone anchor, non-bioabsorbable
No Description
DERMARITE INDUSTRIES LLC
00259E
In Commercial Distribution

  • 00714196259448 ()
  • 01714196259447 ()


  • Exudate-absorbent dressing, non-gel, non-antimicrobial
No Description
DERMARITE INDUSTRIES LLC
00229E
In Commercial Distribution

  • 00714196229229 ()
  • 01714196229228 ()


  • Exudate-absorbent dressing, non-gel, non-antimicrobial
A wound cover that wraps around the leg and foot which is intended to be used as an initial, short-term treatment after injury that consists of an absorbent pad (e.g., gauze, cotton wool, lint, cellulose) The device is intended for use in the home or a clinical setting to protect wounds, arrest bleeding. This is a single-use device.
SUN SCIENTIFIC, INC.
EC6150
In Commercial Distribution

  • 00850051939473 ()
ECWF100

  • First aid absorbent pad/bandage
< 1 ... 14 15 16 17 18 ... 250 >