SEARCH RESULTS FOR: Origin(1423 results)
Tyke is intended for use in neonates and infants for repair of pericardial structures, as an epicardial covering for damaged or repaired cardiac structures, as a patch material for intracardiac defects, septal defect and annulus repair, suture-line buttressing, and cardiac repair.
Elutia Med LLC
CMCV-098-204
In Commercial Distribution
- 10859389005109 ()
- 00859389005102 ()
- Height: 4 Centimeter
- Width: 7 Centimeter
- Cardiovascular patch, animal-derived
VasCure for Carotid Repair is indicated for use as a patch material for vascular reconstruction and repair of the carotid artery, including patch closure following carotid endarterectomy and suture-line buttressing.
Elutia Med LLC
CMCV-073-609
In Commercial Distribution
- 10859389005093 ()
- 00859389005096 ()
- Height: 1 Centimeter
- Width: 10 Centimeter
- Cardiovascular patch, animal-derived
VasCure for Carotid Repair is indicated for use as a patch material for vascular reconstruction and repair of the carotid artery, including patch closure following carotid endarterectomy and suture-line buttressing.
Elutia Med LLC
CMCV-072-606
In Commercial Distribution
- 10859389005086 ()
- 00859389005089 ()
- Width: 10 Centimeter
- Height: 2 Centimeter
- Cardiovascular patch, animal-derived
The CanGaroo® Envelope is intended to securely hold a cardiac implantable electronic device or an implantable neurostimulator to create a stable environment when implanted in the body. The cardiac implantable electronic devices that may be used with the CanGaroo® Envelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. The implantable neurostimulator devices that may be used with the CanGaroo® Envelope include vagus nerve stimulators, spinal cord
neuromodulators, deep brain stimulators and sacral nerve stimulators.
Elutia Med LLC
CMCV-009-XLG
In Commercial Distribution
- 10859389005079 ()
- 00859389005072 ()
- Extra Large
- Cardiovascular patch, animal-derived
The CanGaroo® Envelope is intended to securely hold a cardiac implantable electronic device or an implantable neurostimulator to create a stable environment when implanted in the body. The cardiac implantable electronic devices that may be used with the CanGaroo® Envelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. The implantable neurostimulator devices that may be used with the CanGaroo® Envelope include vagus nerve stimulators, spinal cord
neuromodulators, deep brain stimulators and sacral nerve stimulators.
Elutia Med LLC
CMCV-009-LRG
In Commercial Distribution
- 10859389005062 ()
- 00859389005065 ()
- Large
- Cardiovascular patch, animal-derived
ProxiCor for Cardiac Tissue Repair is indicated for use as an intracardiac patch or pledget for tissue repair and suture-line buttressing.
Elutia Med LLC
CMCV-067-404
In Commercial Distribution
- 10859389005055 ()
- 00859389005058 ()
- Width: 7 Centimeter
- Height: 4 Centimeter
- Cardiovascular patch, animal-derived
ProxiCor for Cardiac Tissue Repair is indicated for use as an intracardiac patch or pledget for tissue repair and suture-line buttressing.
Elutia Med LLC
CMCV-064-401
In Commercial Distribution
- 10859389005048 ()
- 00859389005041 ()
- Width: 7 Centimeter
- Height: 10 Centimeter
- Cardiovascular patch, animal-derived
The CanGaroo® Envelope is intended to securely hold a cardiac implantable electronic device or an implantable neurostimulator to create a stable environment when implanted in the body. The cardiac implantable electronic devices that may be used with the CanGaroo® Envelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. The implantable neurostimulator devices that may be used with the CanGaroo® Envelope include vagus nerve stimulators, spinal cord
neuromodulators, deep brain stimulators and sacral nerve stimulators.
Elutia Med LLC
CMCV-009-MED
In Commercial Distribution
- 10859389005031 ()
- 00859389005034 ()
- Medium
- Cardiovascular patch, animal-derived
The CanGaroo® Envelope is intended to securely hold a cardiac implantable electronic device or an implantable neurostimulator to create a stable environment when implanted in the body. The cardiac implantable electronic devices that may be used with the CanGaroo® Envelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. The implantable neurostimulator devices that may be used with the CanGaroo® Envelope include vagus nerve stimulators, spinal cord
neuromodulators, deep brain stimulators and sacral nerve stimulators.
Elutia Med LLC
CMCV-009-SML
In Commercial Distribution
- 10859389005024 ()
- 00859389005027 ()
- Small
- Cardiovascular patch, animal-derived
ProxiCor for Pericardial Closure is a decellularized natural scaffold for repairing the pericardium following cardiac surgery.
Elutia Med LLC
CMCV-060-402
In Commercial Distribution
- 10859389005017 ()
- 00859389005010 ()
- Width: 7.0 Centimeter
- Height: 15.0 Centimeter
- Cardiovascular patch, animal-derived
ProxiCor for Pericardial Closure is a decellularized natural scaffold for repairing the pericardium following cardiac surgery.
Elutia Med LLC
CMCV-059-401
In Commercial Distribution
- 00859389005003 ()
- 10859389005000 ()
- Height: 10 Centimeter
- Width: 7 Centimeter
- Cardiovascular patch, animal-derived
Digital Transmitter for the Avery Breathing Pacemaker System
Avery Biomedical Devices Inc
NeurostimulatorTransmitter Digital
In Commercial Distribution
- 00850252006066 ()
Spirit
- Extramuscular diaphragm/phrenic nerve electrical stimulation system
No Description
Avery Biomedical Devices Inc
Transtelephonic Monitor
Not in Commercial Distribution
- 00850252006059 ()
TTM
- Extramuscular diaphragm/phrenic nerve electrical stimulation system
(902A) 2.0 m Lead Length
Avery Biomedical Devices Inc
External Antenna
In Commercial Distribution
- 00850252006042 ()
902AL
- Extramuscular diaphragm/phrenic nerve electrical stimulation system
(902A) 1.0 m Lead Length
Avery Biomedical Devices Inc
External Antenna
In Commercial Distribution
- 00850252006035 ()
902A
- Extramuscular diaphragm/phrenic nerve electrical stimulation system
No Description
Avery Biomedical Devices Inc
Neurostimulator Electrode Implant
In Commercial Distribution
- 00850252006028 ()
E377-05
- Extramuscular diaphragm/phrenic nerve electrical stimulation system
No Description
Avery Biomedical Devices Inc
Neurostimulator Receiver Implant
In Commercial Distribution
- 00850252006011 ()
I-110A
- Extramuscular diaphragm/phrenic nerve electrical stimulation system
No Description
Avery Biomedical Devices Inc
Neurostimulator Transmitter
In Commercial Distribution
- 00850252006004 ()
MARK IV
- Extramuscular diaphragm/phrenic nerve electrical stimulation system
Epicel (cultured epidermal autografts) is an aseptically processed wound dressing composed of the patient’s own (autologous) keratinocytes grown ex vivo in the presence of proliferation-arrested, murine (mouse) fibroblasts. Epicel consists of sheets of proliferative, autologous keratinocytes, ranging from 2 to 8 cell layers thick and is referred to as a cultured epidermal autograft. Each graft of Epicel is attached to petrolatum gauze backing with titanium surgical clips and measures a minimum of 50 cm2 in area.
Epicel is authorized by Federal law for use in adult and pediatric patients who have deep dermal or full-thickness burns comprising a total body surface area greater than or equal to 30%. Epicel may be used in conjunction with split-thickness autografts, or alone in patients for whom split-thickness autografts may not be an option due to the severity and extent of their burns.
VERICEL CORPORATION
N/A
In Commercial Distribution
- W41020AU201S1969 ()
- Area/Surface Area: 50 Square centimeter
- Cultured skin autograft/xenograft
Epicel (cultured epidermal autografts) is an aseptically processed wound dressing composed of the patient’s own (autologous) keratinocytes grown ex vivo in the presence of proliferation-arrested, murine (mouse) fibroblasts. Epicel consists of sheets of proliferative, autologous keratinocytes, ranging from 2 to 8 cell layers thick and is referred to as a cultured epidermal autograft. Each graft of Epicel is attached to petrolatum gauze backing with titanium surgical clips and measures approximately 50 cm2 in area.
Epicel is authorized by Federal law for use in adult and pediatric patients who have deep dermal or full-thickness burns comprising a total body surface area greater than or equal to 30%. Epicel may be used in conjunction with split-thickness autografts, or alone in patients for whom split-thickness autografts may not be an option due to the severity and extent of their burns.
VERICEL CORPORATION
0
In Commercial Distribution
- W41020AU201P0001 ()
- Area/Surface Area: 50 Square centimeter
- Cultured skin autograft/xenograft