Areta 14-Panel Drug Test Cup (25 Test Kit): AMP,BAR,BUP,BZO,COC,MAMP (MET),MDMA,MTD,OPI2000 (OPI),OXY,PCP,PPX,TCA,THC

Areta 14-Panel Drug Test Cup (5 Test Kit): AMP,BAR,BUP,BZO,COC,MAMP (MET),MDMA,MTD,OPI2000 (OPI),OXY,PCP,PPX,TCA,THC

Areta 12 Panel Drug Test Cup (5 tests kit): BUP,THC,COC,MOP,MET,OXY,AMP,BAR,BZO,MTD,MDMA,PCP

Easy@Home Pregnancy Test Strip (Bulk)

The sleep remote is an external device that is about the size of a cell phone and is used by the patient to activate the Inspire system before they go to sleep. The patient places the remote over the implanted IPG site, and uses push buttons on top of the programmer to: a.) turn the therapy ON or OFF, b.) temporarily suspend therapy, or c.) make adjustments to the stimulation strength (within limits set by the physician). The patient’s sleep remote also allows patients to check the status of the IPG battery. There are both visual and audio indicators that provide information on the IPG status (therapy ON/OFF, therapy paused, stimulation level and battery status). The Inspire sleep remote will only communicate with the Inspire IPG.

The sleep remote is an external device that is about the size of a cell phone and is used by the patient to activate the Inspire system before they go to sleep. The patient places the remote over the implanted IPG site, and uses push buttons on top of the programmer to: a.) turn the therapy ON or OFF, b.) temporarily suspend therapy, or c.) make adjustments to the stimulation strength (within limits set by the physician). The patient’s sleep remote also allows patients to check the status of the IPG battery. There are both visual and audio indicators that provide information on the IPG status (therapy ON/OFF, therapy paused, stimulation level and battery status). The Inspire sleep remote will only communicate with the Inspire IPG.

The sleep remote is an external device that is about the size of a cell phone and is used by the patient to activate the Inspire system before they go to sleep. The patient places the remote over the implanted IPG site, and uses push buttons on top of the programmer to: a.) turn the therapy ON or OFF, b.) temporarily suspend therapy, or c.) make adjustments to the stimulation strength (within limits set by the physician). The patient’s sleep remote also allows patients to check the status of the IPG battery. There are both visual and audio indicators that provide information on the IPG status (therapy ON/OFF, therapy paused, stimulation level and battery status). The Inspire sleep remote will only communicate with the Inspire IPG.

The Model 2740 physician programmer is designed for use by a physician to non invasively interrogateand program the IPG. It is the only component in the Inspire system that contains software. Thisprogrammer consists of a tablet computer and a telemetry cable. The telemetry head communicateswith the IPG through the skin via short range radio frequency (RF) telemetry, telemetry communicationallows the physician to noninvasively interrogate and program the IPG. The telemetry head is poweredby a wall outlet connection and wirelessly communicates (via wireless Bluetooth link) with the physicianprogrammer tablet. The physician programmer has the capability to monitor respiratory waveforms,program stimulation modes, adjust stimulation parameter values, and store waveforms and settings.

The Model 2740 physician programmer is designed for use by a physician to non invasively interrogateand program the IPG. It is the only component in the Inspire system that contains software. Thisprogrammer consists of a tablet computer and a telemetry cable. The telemetry head communicateswith the IPG through the skin via short range radio frequency (RF) telemetry, telemetry communicationallows the physician to noninvasively interrogate and program the IPG. The telemetry head is poweredby a wall outlet connection and wirelessly communicates (via wireless Bluetooth link) with the physicianprogrammer tablet. The physician programmer has the capability to monitor respiratory waveforms,program stimulation modes, adjust stimulation parameter values, and store waveforms and settings.

The Model 2740 physician programmer is designed for use by a physician to non invasively interrogateand program the IPG. It is the only component in the Inspire system that contains software. Thisprogrammer consists of a tablet computer and a telemetry cable. The telemetry head communicateswith the IPG through the skin via short range radio frequency (RF) telemetry, telemetry communicationallows the physician to noninvasively interrogate and program the IPG. The telemetry head is poweredby a wall outlet connection and wirelessly communicates (via wireless Bluetooth link) with the physicianprogrammer tablet. The physician programmer has the capability to monitor respiratory waveforms,program stimulation modes, adjust stimulation parameter values, and store waveforms and settings.

The Model 2740 physician programmer is designed for use by a physician to non invasively interrogateand program the IPG. It is the only component in the Inspire system that contains software. Thisprogrammer consists of a tablet computer and a telemetry cable. The telemetry head communicateswith the IPG through the skin via short range radio frequency (RF) telemetry, telemetry communicationallows the physician to noninvasively interrogate and program the IPG. The telemetry head is poweredby a wall outlet connection and wirelessly communicates (via wireless Bluetooth link) with the physicianprogrammer tablet. The physician programmer has the capability to monitor respiratory waveforms,program stimulation modes, adjust stimulation parameter values, and store waveforms and settings.

The Model 2740 physician programmer is designed for use by a physician to non‐invasively interrogateand program the IPG. It is the only component in the Inspire system that contains software. Thisprogrammer consists of a tablet computer and a telemetry cable. The telemetry head communicateswith the IPG through the skin via short‐range radio‐frequency (RF) telemetry; telemetry communicationallows the physician to noninvasively interrogate and program the IPG. The telemetry head is poweredby a wall outlet connection and wirelessly communicates (via wireless Bluetooth link) with the physicianprogrammer tablet. The physician programmer has the capability to monitor respiratory waveforms,program stimulation modes, adjust stimulation parameter values, and store waveforms and settings.

The Model 2740 physician programmer is designed for use by a physician to non‐invasively interrogateand program the IPG. It is the only component in the Inspire system that contains software. Thisprogrammer consists of a tablet computer and a telemetry cable. The telemetry head communicateswith the IPG through the skin via short‐range radio‐frequency (RF) telemetry; telemetry communicationallows the physician to noninvasively interrogate and program the IPG. The telemetry head is poweredby a wall outlet connection and wirelessly communicates (via wireless Bluetooth link) with the physicianprogrammer tablet. The physician programmer has the capability to monitor respiratory waveforms,program stimulation modes, adjust stimulation parameter values, and store waveforms and settings.

The Model 2740 physician programmer is designed for use by a physician to non‐invasively interrogateand program the IPG. It is the only component in the Inspire system that contains software. Thisprogrammer consists of a tablet computer and a telemetry cable. The telemetry head communicateswith the IPG through the skin via short‐range radio‐frequency (RF) telemetry; telemetry communicationallows the physician to noninvasively interrogate and program the IPG. The telemetry head is poweredby a wall outlet connection and wirelessly communicates (via wireless Bluetooth link) with the physicianprogrammer tablet. The physician programmer has the capability to monitor respiratory waveforms,program stimulation modes, adjust stimulation parameter values, and store waveforms and settings.

The Model 2740 physician programmer is designed for use by a physician to non‐invasively interrogateand program the IPG. It is the only component in the Inspire system that contains software. Thisprogrammer consists of a tablet computer and a telemetry cable. The telemetry head communicateswith the IPG through the skin via short‐range radio‐frequency (RF) telemetry; telemetry communicationallows the physician to noninvasively interrogate and program the IPG. The telemetry head is poweredby a wall outlet connection and wirelessly communicates (via wireless Bluetooth link) with the physicianprogrammer tablet. The physician programmer has the capability to monitor respiratory waveforms,program stimulation modes, adjust stimulation parameter values, and store waveforms and settings.

The Model 2740 physician programmer is designed for use by a physician to non-invasively interrogate and program the IPG. It is the only component in the Inspire system that contains software. This programmer consists of a tablet computer and a telemetry cable. The telemetry head communicates with the IPG through the skin via short-range radio-frequency (RF) telemetry; telemetry communication allows the physician to noninvasively interrogate and program the IPG. The telemetry head is powered by a wall outlet connection and wirelessly communicates (via wireless Bluetooth link) with the physician programmer tablet. The physician programmer has the capability to monitor respiratory waveforms, program stimulation modes, adjust stimulation parameter values, and store waveforms and settings. This data can also be printed via a wireless Bluetooth link to a commercial printer.

The Model 2740 physician programmer is designed for use by a physician to non-invasively interrogate and program the IPG. It is the only component in the Inspire system that contains software. This programmer consists of a tablet computer and a telemetry cable. The telemetry head communicates with the IPG through the skin via short-range radio-frequency (RF) telemetry; telemetry communication allows the physician to noninvasively interrogate and program the IPG. The telemetry head is powered by a wall outlet connection and wirelessly communicates (via wireless Bluetooth link) with the physician programmer tablet. The physician programmer has the capability to monitor respiratory waveforms, program stimulation modes, adjust stimulation parameter values, and store waveforms and settings. This data can also be printed via a wireless Bluetooth link to a commercial printer.

The Model 2740 physician programmer is designed for use by a physician to non-invasively interrogate and program the IPG. It is the only component in the Inspire system that contains software. This programmer consists of a tablet computer and a telemetry cable. The telemetry head communicates with the IPG through the skin via short-range radio-frequency (RF) telemetry; telemetry communication allows the physician to noninvasively interrogate and program the IPG. The telemetry head is powered by a wall outlet connection and wirelessly communicates (via wireless Bluetooth link) with the physician programmer tablet. The physician programmer has the capability to monitor respiratory waveforms, program stimulation modes, adjust stimulation parameter values, and store waveforms and settings. This data can also be printed via a wireless Bluetooth link to a commercial printer.

The Model 3024 Inspire II IPG contains electronics and a battery that are sealed inside a titanium case. The IPG is implanted subcutaneously below the clavicle in the upper chest, and connects to the stimulation lead and sensing lead. The IPG has multiple programmable parameters that can be adjusted for a particular patient. Adjustments may be made to the sensing circuits to vary the timing of stimulation pulses and to the stimulation circuits to adjust the energy and duration of stimulation pulses. These adjustments provide the ability to optimize the opening of the upper airway. Based on typical settings from the STAR pivotal trial the longevity of the IPG’s battery will average 10 years. The Model 3024 IPG was originally developed by Medtronic and utilizes the same platform as Medtronic’s Itrel® 3 IPG which is FDA approved for other neurostimulation therapies. Figure 9 provides a photograph of the Model 3024 IPG.

The Model 3024 Inspire II IPG contains electronics and a battery that are sealed inside a titanium case. The IPG is implanted subcutaneously below the clavicle in the upper chest, and connects to the stimulation lead and sensing lead. The IPG has multiple programmable parameters that can be adjusted for a particular patient. Adjustments may be made to the sensing circuits to vary the timing of stimulation pulses and to the stimulation circuits to adjust the energy and duration of stimulation pulses. These adjustments provide the ability to optimize the opening of the upper airway. Based on typical settings from the STAR pivotal trial the longevity of the IPG’s battery will average 10 years. The Model 3024 IPG was originally developed by Medtronic and utilizes the same platform as Medtronic’s Itrel® 3 IPG which is FDA approved for other neurostimulation therapies. Figure 9 provides a photograph of the Model 3024 IPG.

The patient programmer is an external device that is about the size of a cell phone or PDA, and is used by the patient to activate the Inspire system before they go to sleep. The patient places the programmer over the implanted IPG site, and uses push buttons on top of the programmer to: a.) turn the therapy ON or OFF, b.) temporarily suspend therapy, or c.) make adjustments to the stimulation amplitude (within limits set by the physician). The patient programmer also allows patients to check the status of the IPG battery. There are both visual and audio indicators that provide confirmation of IPG status (Therapy ON/OFF and Battery Status). The patient programmer will only communicate with the Inspire system IPG

The stimulation lead incorporates a cuff segment that includes three electrodes in a guarded-bipolar configuration, which means the center electrode is connected to one pole of the stimulation (e.g., negative pole), and is flanked on each side by two electrodes connected to the opposite pole of stimulation (e.g., positive pole). It is packaged with a tunneling rod to facilitate the implant procedure. The cuff is surgically positioned around a patient’s hypoglossal nerve, and the connector end of the lead is connected to the IPG. The cuff electrodes apply electrical current that stimulates the nerve causing the tongue to move forward. The tongue movement (via genioglossus and other tongue protrusor muscle contraction) serves to maintain an open airway. The figure below provides an illustration of the Model 4063 stimulation lead.

The stimulation lead incorporates a cuff segment that includes three electrodes in a guarded-bipolar configuration, which means the center electrode is connected to one pole of the stimulation (e.g., negative pole), and is flanked on each side by two electrodes connected to the opposite pole of stimulation (e.g., positive pole). It is packaged with a tunneling rod to facilitate the implant procedure. The cuff is surgically positioned around a patient’s hypoglossal nerve, and the connector end of the lead is connected to the IPG. The cuff electrodes apply electrical current that stimulates the nerve causing the tongue to move forward. The tongue movement (via genioglossus and other tongue protrusor muscle contraction) serves to maintain an open airway. The figure below provides an illustration of the Model 4063 stimulation lead.

The sensing lead incorporates a differential pressure sensor that detects respiratory cycles. The connector end of the lead is connected to the IPG. The sensor is implanted in between the intercostal muscle layers. The device senses relative pressure variations that correspond to the respiration cycle. The pressure waveform is monitored by the IPG and triggers stimulation therapy synchronous with inspiration

The sensing lead incorporates a differential pressure sensor that detects respiratory cycles. The connector end of the lead is connected to the IPG. The sensor is implanted in between the intercostal muscle layers. The device senses relative pressure variations that correspond to the respiration cycle. The pressure waveform is monitored by the IPG and triggers stimulation therapy synchronous with inspiration.

The NeuroPace® Remote Monitor Phone Accessories package contains 1 External Modem, 1 Telephone Cord, 1 Telephone Line Splitter.

The Connector Cover package contains 1 Connector Cover, 2 Connector Plugs, 1 Lead Strain Relief and 1 Torque Driver.

The Craniectomy Template package contains 1 Craniectomy Template, 1 Lead Strain Relief and 1 Torque Driver.

The NeuroPace® Depth Lead package contains 1 Depth Lead, 2 Lead Caps, 4 Suture Sleeves, 1 Stop Gauge and 1 Tunneling Tool Straw.

The Ferrule package contains 1 Ferrule, 1 Ferrule Clamp and 1 Torque Driver.

The NeuroPace® RNS® Neurostimulator package contains 1 RNS® Neurostimulator, 1 Connector Cover, 1 Ferrule, 1 Ferrule Clamp, 1 Lead Strain Relief and 1 Torque Driver.

GlucanPro Cream is intended to be used as an aid in the management of superficial abrasions, scrapes, cuts and lacerations; minor burns and scalds, partial and full thickness wounds, and irritations of the skin. GlucanPro Cream may also be used, under the supervision/direction of a health care professional for pressure ulcers; venous, diabetic, and arterial ulcers; partial thickness burns; donor graft sites; and surgical wounds.GlucanPro Cream provides a moist environment which supports in the autolytic debridement of wounds with scattered areas of necrosis and slough.

GlucanPro Cream is intended to be used as an aid in the management of superficial abrasions, scrapes cuts and lacerations; minor burns and scalds, partial and full thickness wounds, and irritations of the skin. GlucanPro Cream may also be used, under the supervision/direction of a health care professional for pressure ulcers, venous, diabetic and arterial ulcers; partial thickness burns; donor graft sites; and surgical wounds.GlucanPro Cream provides a moist environment which supports in the autolytic debridement of wounds with scattered areas of necrosis and slough.

GlucanPro Cream is intended to be used as an aid in the management of superficial abrasions, scrapes, cuts and lacerations; minor burns and scalds, partial and full thickness wounds, and irritations of the skin. GlucanPro Cream may also be used, under the supervision/direction of a health care professional for pressure ulcers; venous, diabetic, and arterial ulcers; partial thickness burns; donor graft sites; and surgical wounds.GlucanPro Cream provides a moist environment which supports in the autolytic debridement of wounds with scattered areas of necrosis and slough.

GlucanPro Cream is intended to be used as an aid in the management of superficial abrasions, scrapes, cuts and lacerations; minor burns and scalds, partial and full thickness wounds, and irritations of the skin. GlucanPro Cream may also be used, under the supervision/direction of a health care professional for pressure ulcers; venous, diabetic, and arterial ulcers; partial thickness burns; donor graft sites; and surgical wounds.GlucanPro Cream provides a moist environment which supports in the autolytic debridement of wounds with scattered areas of necrosis and slough.