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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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No Description
CABLES AND SENSORS, LLC
F1720DC1818050
In Commercial Distribution

  • B817F1720DC18180501 ()
  • B817F1720DC18180500 ()


  • Blood pressure cuff, single-use
No Description
CABLES AND SENSORS, LLC
F1720DC1718050
In Commercial Distribution

  • B817F1720DC17180501 ()
  • B817F1720DC17180500 ()


  • Blood pressure cuff, single-use
No Description
CABLES AND SENSORS, LLC
F1720DC0808050
In Commercial Distribution

  • B817F1720DC08080501 ()
  • B817F1720DC08080500 ()


  • Blood pressure cuff, single-use
No Description
CABLES AND SENSORS, LLC
10208
In Commercial Distribution

  • B817102081 ()
  • B817102080 ()


  • Pulse oximeter probe, single-use
No Description
CABLES AND SENSORS, LLC
10167
In Commercial Distribution

  • B817101671 ()
  • B817101670 ()


  • Blood pressure cuff, single-use
No Description
CABLES AND SENSORS, LLC
10166
In Commercial Distribution

  • B817101661 ()
  • B817101660 ()


  • Blood pressure cuff, single-use
No Description
CABLES AND SENSORS, LLC
10165
In Commercial Distribution

  • B817101651 ()
  • B817101650 ()


  • Blood pressure cuff, single-use
No Description
CABLES AND SENSORS, LLC
10164
In Commercial Distribution

  • B817101641 ()
  • B817101640 ()


  • Blood pressure cuff, single-use
No Description
CABLES AND SENSORS, LLC
10163
In Commercial Distribution

  • B817101631 ()
  • B817101630 ()


  • Blood pressure cuff, single-use
No Description
CABLES AND SENSORS, LLC
10130
In Commercial Distribution

  • B817101301 ()
  • B817101300 ()


  • Blood pressure cuff, single-use
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