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The Neuroguard IEP System consists of three main components:
• A self-expanding nitinol stent
• A delivery catheter which includes a post-dilation balloon and activation handle
• Embolic protection filter that is integrated at the distal end of the delivery system
Contego Medical, Inc.
NG-0640-140-2
In Commercial Distribution
- 00851616007590 ()
NG-0640-140-2
- Peripheral angioplasty balloon catheter, basic
- Carotid artery embolic protection system
- Bare-metal carotid artery stent
The Neuroguard IEP System consists of three main components:
• A self-expanding nitinol stent
• A delivery catheter which includes a post-dilation balloon and activation handle
• Embolic protection filter that is integrated at the distal end of the delivery system
Contego Medical, Inc.
NG-0630-140-2
In Commercial Distribution
- 00851616007583 ()
NG-0630-140-2
- Bare-metal carotid artery stent
- Carotid artery embolic protection system
- Peripheral angioplasty balloon catheter, basic
The BioFilmChip Microarray consists of a polyester film coated with proprietary multi-layer components designed for DNA analysis as part of AvertD™, a prescription, qualitative genotyping test used to detect and identify 15 genetic polymorphisms in genomic DNA.
AUTOGENOMICS, INC
03-1560-01
In Commercial Distribution
- 10850009370218 ()
- 30850009370212 ()
03-1560-01
- Opioid use disorder (OUD) genotyping IVD, kit, nucleic acid technique (NAT)
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-02
In Commercial Distribution
- M727PADPAK02 ()
Pad-Pak-02
- Non-rechargeable public semi-automated external defibrillation electrode, paediatric
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
Intellisense Pediatric Defibrillation Pads, reduced energy, for Powerheart G5 (up to 8 years of age or 55 lbs)
Zoll Medical Corporation
XELAED003B
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
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
XELAED003B
In Commercial Distribution
- 00812394020515 ()
XELAED003B
- External defibrillation electrode, paediatric, single-use