SEARCH RESULTS FOR: (*what is fsi pso billmatrix*)(155610 results)
Only the first 10,000 results were returned. Filter these results or refine your query. Some pre-built queries with more than 10,000 results are available for download.
"The GSS Pedicle Screw System is a top-loading multiple component, posterior spinal fixation system which consists of pedicle screws, rods, locking spacer, and a transverse (cross) linking mechanism. The GSS Pedicle Screw System will allow surgeons to build a spinal implant construct to stabilize and promote spinal fusion. The GSS Pedicle Screw System implant components are supplied non-sterile, single use and fabricated from titanium alloy (Ti-6AI-4V ELI) that conforms to ASTM F136. Various sizes of these implants are available. Specialized instruments are available for the application and removal of the GSS Pedicle Screw System.
The GSS Pedicle Screw System is a pedicle screw system indicated for the treatment of severe Spondylolisthesis (Grade 3 and 4) of the L5-SI vertebra in skeletally mature patients receiving fusion by autogenous bone graft having implants attached to the lumbar and sacral spine (L3 to sacrum) with removal of the implants after the attainment of a solid fusion."
GS Medical Co., Ltd.
GS0120-0021
In Commercial Distribution
- 08806378329789 ()
GS0120-0021
- Bone-screw internal spinal fixation system, non-sterile
"The GSS Pedicle Screw System is a top-loading multiple component, posterior spinal fixation system which consists of pedicle screws, rods, locking spacer, and a transverse (cross) linking mechanism. The GSS Pedicle Screw System will allow surgeons to build a spinal implant construct to stabilize and promote spinal fusion. The GSS Pedicle Screw System implant components are supplied non-sterile, single use and fabricated from titanium alloy (Ti-6AI-4V ELI) that conforms to ASTM F136. Various sizes of these implants are available. Specialized instruments are available for the application and removal of the GSS Pedicle Screw System.
The GSS Pedicle Screw System is a pedicle screw system indicated for the treatment of severe Spondylolisthesis (Grade 3 and 4) of the L5-SI vertebra in skeletally mature patients receiving fusion by autogenous bone graft having implants attached to the lumbar and sacral spine (L3 to sacrum) with removal of the implants after the attainment of a solid fusion."
GS Medical Co., Ltd.
GS0120-0019
In Commercial Distribution
- 08806378329772 ()
GS0120-0019
- Bone-screw internal spinal fixation system, non-sterile
"The GSS Pedicle Screw System is a top-loading multiple component, posterior spinal fixation system which consists of pedicle screws, rods, locking spacer, and a transverse (cross) linking mechanism. The GSS Pedicle Screw System will allow surgeons to build a spinal implant construct to stabilize and promote spinal fusion. The GSS Pedicle Screw System implant components are supplied non-sterile, single use and fabricated from titanium alloy (Ti-6AI-4V ELI) that conforms to ASTM F136. Various sizes of these implants are available. Specialized instruments are available for the application and removal of the GSS Pedicle Screw System.
The GSS Pedicle Screw System is a pedicle screw system indicated for the treatment of severe Spondylolisthesis (Grade 3 and 4) of the L5-SI vertebra in skeletally mature patients receiving fusion by autogenous bone graft having implants attached to the lumbar and sacral spine (L3 to sacrum) with removal of the implants after the attainment of a solid fusion."
GS Medical Co., Ltd.
GS0120-0018
In Commercial Distribution
- 08806378329765 ()
GS0120-0018
- Bone-screw internal spinal fixation system, non-sterile
"The GSS Pedicle Screw System is a top-loading multiple component, posterior spinal fixation system which consists of pedicle screws, rods, locking spacer, and a transverse (cross) linking mechanism. The GSS Pedicle Screw System will allow surgeons to build a spinal implant construct to stabilize and promote spinal fusion. The GSS Pedicle Screw System implant components are supplied non-sterile, single use and fabricated from titanium alloy (Ti-6AI-4V ELI) that conforms to ASTM F136. Various sizes of these implants are available. Specialized instruments are available for the application and removal of the GSS Pedicle Screw System.
The GSS Pedicle Screw System is a pedicle screw system indicated for the treatment of severe Spondylolisthesis (Grade 3 and 4) of the L5-SI vertebra in skeletally mature patients receiving fusion by autogenous bone graft having implants attached to the lumbar and sacral spine (L3 to sacrum) with removal of the implants after the attainment of a solid fusion."
GS Medical Co., Ltd.
GS0120-0017
In Commercial Distribution
- 08806378329758 ()
GS0120-0017
- Bone-screw internal spinal fixation system, non-sterile
BRUSH, CLEANING, APPLIANCE, URINARY, OSTOMY, SMALL PARTS, STAINLESS STEEL, NYLON BRISTLES, 8" (20CM)
This brush is made with durable, white-nylon bristles and a malleable, twisted, stainless-steel wire body. It may be shaped to fit almost any contour and is especially good for removing uric crystal build-ups from within urinary and ostomy appliances. May be used with Urocare® reusable Latex urinary leg bags, Urocare® Urinary Drainage Bottle, Urocare® Male Urinal Systems, Urocare® Male Urinal Kits or any other urinary or ostomy appliance that has small parts, tight corners, small holes and other hard to reach areas that need periodic brushing to loosen calcium and uric crystal build-ups.
Rinsing alone does not clean a urinary or ostomy appliance and the use of vinegar, bleaches or toilet bowl cleaners only hardens, distorts and damages rubber, latex and plastic parts—not to mention the unpleasant and embarrassing odors often created by the use of these chemicals. Urocare® recommends the use of Urolux® urinary and ostomy appliance cleanser and deodorant for cleaning latex or rubber urinary leg bags, male urinal sheaths, urinary drainage bottles, urinary drainage and extension tubing or any other reusable urinary or ostomy appliance. Urolux® is a concentrated solution specifically formulated to clean and deodorize rubber, latex or plastic urinary and ostomy appliances. Crystal build-ups are dissolved and unpleasant odors are eliminated. Don't let corrosion happen to your urinary or ostomy appliance... Use Urolux!
UROCARE PRODUCTS, INC.
7003
In Commercial Distribution
- 10792293070033 ()
- 00792293070036 ()
- Bristles: 0.25" O.D. x 0.75" O.D. x 3.38" Bristles: (0.6cm Ø x 1.9cm Ø x 8.6cm)
- Length: 20 Centimeter
- Outer Diameter: 1.9 Centimeter
- Length: 8.00 Inch
- Outer Diameter: 0.75 Inch
- Weight: 0.40 Pound
7003
- Endoscope cleaning brush, reusable
- Penis/scrotum wearable urinal
- Non-wearable adult urine collection bag, open-ended
- Open-ended wearable urine collection bag, non-sterile
- Hand-held urinal, reusable
- Urinary incontinence penis sheath/port, single-use
INTENDED USE/ CONTRAINDICATIONS
PremierPro™ Air Transfer Mats are indicated for patients:
Who are unable to transfer or turn by their own effort, both assisted and unassisted.
Whose size and weight present possible risks to caregivers involved in the transfer of the patient.
PRECAUTIONS & WARNINGS
Use two or more caregivers during patient transfers.
Do not use transfer mat until user manual is reviewed.
Do not leave patient unattended on inflated transfer mat.
Do not attempt to move patient on uninflated transfer mat.
The maximum safe working load for all PremierPro™ Air Transfer Mats is l,000lbs (450kg).
AIR SUPPLY
Air supply units may be compatible with Premier™ Air Transfer Mats if they provide 3 psi pressure and 80 cfm capacity. The hose used may be a standard 1.75" diameter hose that may be secured with a snap fastener or hook & loop fastener. Always refer the air supply unit's operating instructions, observing all precautions and warnings. All safety guidelines within the air supply unit's operating instructions should be followed.
MRI SAFETY
PremierPro™ Air Transfer Mats may be used in situations that require transferring patients undergoing Magnetic Resonance Imaging (MRI). PremierPro™ Air Transfer Mats have been evaluated for use with MRI and have been determined to be safe for use. This conclusion is based on the following factors:
Materials of construction for top and bottom fabrics include Nylon, PVC and Mesh.
Safety strap buckles are constructed from Polypropylene.
Air supply fasteners are manufactured from non-ferrous metal.
Air supply fasteners are not in the radio frequency field or the field of imaging and will not cause artifacts.
Evaluation of these factors indicates PremierPro™ Air Transfer Mats are safe when used with patients undergoing MRI.
CLEANING
The PremierPro™ Disposable Air Transfer Mat is not intended to be laundered and reused. Check Local, State and Federal Guidelines before disposing of this product.
SVS LLC
3711
In Commercial Distribution
- 10818566019216 ()
- 00818566019219 ()
- Length: 39 Inch
3711
- Patient transfer system, powered
INTENDED USE/ CONTRAINDICATIONS
PremierPro™ Air Transfer Mats are indicated for patients:
Who are unable to transfer or turn by their own effort, both assisted and unassisted.
Whose size and weight present possible risks to caregivers involved in the transfer of the patient.
PRECAUTIONS & WARNINGS
Use two or more caregivers during patient transfers.
Do not use transfer mat until user manual is reviewed.
Do not leave patient unattended on inflated transfer mat.
Do not attempt to move patient on uninflated transfer mat.
The maximum safe working load for all PremierPro™ Air Transfer Mats is l,000lbs (450kg).
AIR SUPPLY
Air supply units may be compatible with Premier™ Air Transfer Mats if they provide 3 psi pressure and 80 cfm capacity. The hose used may be a standard 1.75" diameter hose that may be secured with a snap fastener or hook & loop fastener. Always refer the air supply unit's operating instructions, observing all precautions and warnings. All safety guidelines within the air supply unit's operating instructions should be followed.
MRI SAFETY
PremierPro™ Air Transfer Mats may be used in situations that require transferring patients undergoing Magnetic Resonance Imaging (MRI). PremierPro™ Air Transfer Mats have been evaluated for use with MRI and have been determined to be safe for use. This conclusion is based on the following factors:
Materials of construction for top and bottom fabrics include Nylon, PVC and Mesh.
Safety strap buckles are constructed from Polypropylene.
Air supply fasteners are manufactured from non-ferrous metal.
Air supply fasteners are not in the radio frequency field or the field of imaging and will not cause artifacts.
Evaluation of these factors indicates PremierPro™ Air Transfer Mats are safe when used with patients undergoing MRI.
CLEANING
The PremierPro™ Disposable Air Transfer Mat is not intended to be laundered and reused. Check Local, State and Federal Guidelines before disposing of this product.
SVS LLC
3710
In Commercial Distribution
- 10818566019209 ()
- 00818566019202 ()
- Length: 34 Inch
3710
- Patient transfer system, powered
INTENDED USE/ CONTRAINDICATIONS
PremierPro™ Air Transfer Mats are indicated for patients:
Who are unable to transfer or turn by their own effort, both assisted and unassisted.
Whose size and weight present possible risks to caregivers involved in the transfer of the patient.
PRECAUTIONS & WARNINGS
Use two or more caregivers during patient transfers.
Do not use transfer mat until user manual is reviewed.
Do not leave patient unattended on inflated transfer mat.
Do not attempt to move patient on uninflated transfer mat.
The maximum safe working load for all PremierPro™ Air Transfer Mats is l,000lbs (450kg).
AIR SUPPLY
Air supply units may be compatible with Premier™ Air Transfer Mats if they provide 3 psi pressure and 80 cfm capacity. The hose used may be a standard 1.75" diameter hose that may be secured with a snap fastener or hook & loop fastener. Always refer the air supply unit's operating instructions, observing all precautions and warnings. All safety guidelines within the air supply unit's operating instructions should be followed.
MRI SAFETY
PremierPro™ Air Transfer Mats may be used in situations that require transferring patients undergoing Magnetic Resonance Imaging (MRI). PremierPro™ Air Transfer Mats have been evaluated for use with MRI and have been determined to be safe for use. This conclusion is based on the following factors:
Materials of construction for top and bottom fabrics include Nylon, PVC and Mesh.
Safety strap buckles are constructed from Polypropylene.
Air supply fasteners are manufactured from non-ferrous metal.
Air supply fasteners are not in the radio frequency field or the field of imaging and will not cause artifacts.
Evaluation of these factors indicates PremierPro™ Air Transfer Mats are safe when used with patients undergoing MRI.
CLEANING
The PremierPro™ Disposable Air Transfer Mat is not intended to be laundered and reused. Check Local, State and Federal Guidelines before disposing of this product.
SVS LLC
3700
In Commercial Distribution
- 00818566019165 ()
- 10818566019162 ()
- Length: 28 Inch
3700
- Patient transfer system, powered
4.0mm x 38mm Smooth Shaft Poly Screw Assm. The Atoll OCT Spinal System is intended for use as an aid in spine fusion. It consists of screws, hooks, rods, and connectors. These components are available in a variety of sizes to allow for a variety of configurations to better fit each individual patient's pathology. The Atoll OCT Spinal System components are manufactured from medical implant grade titanium alloy Ti-6Al-4V (ELI) per ASTM F-136 or ISO 5832-3.
Seaspine Orthopedics Corporation
16-13-4038
In Commercial Distribution
- 10889981052850 ()
- 4.0mm x 38mm
16-13-4038
- Bone-screw internal spinal fixation system, non-sterile
4.0mm x 30mm Smooth Shaft Poly Screw Assm. The Atoll OCT Spinal System is intended for use as an aid in spine fusion. It consists of screws, hooks, rods, and connectors. These components are available in a variety of sizes to allow for a variety of configurations to better fit each individual patient's pathology. The Atoll OCT Spinal System components are manufactured from medical implant grade titanium alloy Ti-6Al-4V (ELI) per ASTM F-136 or ISO 5832-3.
Seaspine Orthopedics Corporation
16-13-4030
In Commercial Distribution
- 10889981052812 ()
- 4.0mm x 30mm
16-13-4030
- Bone-screw internal spinal fixation system, non-sterile