SEARCH RESULTS FOR: ("Make Dominican School of Philosophy")(70002 results)

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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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Thoraflex Hybrid Plexus 4 Hybrid Stent Device
VASCUTEK LTD
THP3036X100A
In Commercial Distribution

  • 05037881026749 ()

  • Branch Diameter 12,8,10,10
  • Branch Length 150mm
  • Lumen/Inner Diameter: 30 Millimeter
  • Length: 242100 Millimeter
THP3036X100A

  • Synthetic vascular graft
Thoraflex Hybrid Plexus 4 Hybrid Stent Device
VASCUTEK LTD
THP3034X100A
In Commercial Distribution

  • 05037881026732 ()

  • Length: 242100 Millimeter
  • Lumen/Inner Diameter: 30 Millimeter
  • Branch Length 150mm
  • Branch Diameter 12,8,10,10
THP3034X100A

  • Synthetic vascular graft
Thoraflex Hybrid Plexus 4 Hybrid Stent Device
VASCUTEK LTD
THP3032X100A
In Commercial Distribution

  • 05037881026725 ()

  • Length: 242100 Millimeter
  • Branch Length 150mm
  • Branch Diameter 12,8,10,10
  • Lumen/Inner Diameter: 30 Millimeter
THP3032X100A

  • Synthetic vascular graft
DUROLANE is a clear, transparent, viscous gel of highly purified, stabilized, non-animal-derived sodium hyaluronate that is biosynthesized using bacterial fermentation. NASHA® technology is used to stabilize naturally entangled hyaluronic acid (HA) chains to produce a gel. The gel is suspended in phosphate- buffered saline at a concentration of 20 mg/mL. DUROLANE is indicated for the treatment of pain in osteoarthritis (OA) of the knee in patients who have failed to respond adequately to conservative non-pharmacological therapy or simple analgesics, e.g. acetaminophen.
BIOVENTUS LLC
1082020
In Commercial Distribution

  • 00816986020808 ()
  • 10816986020805 ()
  • 89130-2020-1 ()
1082020

  • Synovial fluid supplementation medium
Combined Battery and Electrode Cartridge. Accessory to a therapeutic medical device in the range of Automated External Defibrillators.
HEARTSINE TECHNOLOGIES LTD
Pad-Pak-07
In Commercial Distribution

  • M727PADPAK07 ()
Pad-Pak-07

  • Non-rechargeable public semi-automated external defibrillation electrode, adult
Combined Battery and Electrode Cartridge. Accessory to a therapeutic medical device in the range of Automated External Defibrillators.
HEARTSINE TECHNOLOGIES LTD
Pad-Pak-01
In Commercial Distribution

  • M727PADPAK01 ()
Pad-Pak-01

  • Non-rechargeable public semi-automated external defibrillation electrode, adult
Combined Battery and Electrode Cartridge. Accessory to a therapeutic medical device in the range of Automated External Defibrillators.
HEARTSINE TECHNOLOGIES LTD
Pad-Pak-02
In Commercial Distribution

  • M727PADPAK02 ()
Pad-Pak-02

  • Non-rechargeable public semi-automated external defibrillation electrode, paediatric
Intellisense Pediatric Defibrillation Pads, reduced energy, for Powerheart G5 (up to 8 years of age or 55 lbs)
Zoll Medical Corporation
XELAED003B
In Commercial Distribution

XELAED003B

  • External defibrillation electrode, paediatric, single-use
Intellisense Pediatric Defibrillation Pads, reduced energy, for Powerheart G5 (up to 8 years of age or 55 lbs)
Zoll Medical Corporation
XELAED003A
In Commercial Distribution

XELAED003A

  • External defibrillation electrode, paediatric, single-use
Intellisense Pediatric Defibrillation Pads, reduced energy, for Powerheart G5 (up to 8 years of age or 55 lbs)
Cardiac Science Corporation
XELAED003A
In Commercial Distribution

  • 00812394020171 ()
XELAED003A

  • External defibrillation electrode, paediatric, single-use
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