Abbott 3599 Clinician Manual Download | Manualshive

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Table 2. Ordering information for the EPG

Model

Description

3013

MLTC

1210

Magnet

1203

Box of cleaning cloths

1216

EPG header cap

1213

Pouch with adhesive (5)

1214

Pouch without adhesive and belt (5)

1218

Carrying case

Appendix A: Product Specifications

EPG with Header

The EPG (Model 3599) and EPG header (Model 3032) has the following physical specifications.

Table 3. EPG and EPG header specifications

Height

79.8 mm (3.14 in.)

31

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Summary of Contents for 3599

Page 1: ...Abbott Medical External Pulse Generator Spinal Cord Stimulation Systems Model 3599 Clinician s Manual...

Page 2: ...hysician Indicates a trademark of the Abbott group of companies Indicates a third party trademark which is property of its respective owner Bluetooth and Bluetooth logo are registered trademarks of Bl...

Page 3: ...Contents 11 Getting Started 11 Overview of the EPG Procedure 12 Replacing the EPG Batteries 13 Checking the Status of the EPG Batteries 16 Setting Up Communication Between the EPG and the Clinician P...

Page 4: ...Appendix A Product Specifications 31 EPG with Header 31 Appendix B Regulatory Statements 34 Disposal Guidelines for Battery Powered Devices 34 Statement of FCC Compliance 34 Statement of Compliance W...

Page 5: ...Appendix C Electromagnetic Compatibility Guidelines 40 Radio Frequency Information 45 Appendix D Symbols and Definitions 46 iii...

Page 6: ...iv...

Page 7: ...ions This neurostimulation system is contraindicated for patients who are unable to use the system Neurostimulation should not be used on patients who are poor surgical risks such as those with multip...

Page 8: ...issue at the electrode site and cause severe injury to the patient If use of electrocautery is necessary first turn off the neurostimulation system Implanted cardiac systems Physicians need to be awar...

Page 9: ...torized vehicles machinery or equipment Postural changes Changes in posture or abrupt movements can change the level of stimulation and potentially cause unpleasant sensations Patients should turn sti...

Page 10: ...pathy DPN population System components The use of components not approved for use by Abbott Medical with this system may result in damage to the system and increased risk to the patient Power supply U...

Page 11: ...turn off the EPG and proceed with caution being sure to move through the detector quickly Implantation of multiple leads If multiple leads are implanted leads and extensions should be routed in close...

Page 12: ...omputerized tomography CT scans cobalt machines and linear accelerators If radiation therapy is required disconnect the EPG from the leads or extensions Damage to the system may not be immediately det...

Page 13: ...onsider disabling magnet mode For more information about setting the magnet mode refer to the clinician programmer manual or contact Technical Support Adverse Effects The use of a neurostimulation sys...

Page 14: ...ty of any surgical complication may be greater in patients with diabetes particularly those with inadequate pre operative glycemic control For adverse effects observed in SCS clinical studies refer to...

Page 15: ...pins and needles prickling or even burning called paresthesia Paresthesia may be brief or it may last a long time For more information about the neurostimulation system see the clinician s programmin...

Page 16: ...how the EPG and EPG header features Figure 1 EPG features 1 Connector for multilead trial cable and EPG 1 header 2 Battery compartment panel 2 3 Indicator light 3 Figure 2 EPG header features 1 Button...

Page 17: ...ct documentation the External Pulse Generator 2 Port Header kit Model 3032 contains the following items 1 EPG header 2 CR2450 Batteries Cleaning cloths 1 EPG pouch with adhesive Getting Started This s...

Page 18: ...extensions 3 4 Connect the leads or extensions to the multilead trial cable 4 5 Connect the multilead trial cable to the EPG 5 6 Test the system 6 7 Disconnect the multilead trial cable from the EPG 7...

Page 19: ...as household waste Refer to the guidelines in Appendix B page 34 for more information To replace the batteries 1 Disconnect the EPG header or multilead trial cable from the EPG if either is connected...

Page 20: ...your hand or pressing down on one side of the battery so the opposite side pops up lifting the battery out and repeating the process with the remaining battery 4 Insert a new battery into the battery...

Page 21: ...nserting batteries into the battery compartment 6 Place the battery compartment panel flush to the EPG lining up the tabs with the coordinating 6 indentation Figure 5 Replacing the battery compartment...

Page 22: ...ler app Refer to the clinician s programming or user s controller manual for these directions NOTE Battery life depends on usage and stimulation settings with batteries lasting at least 14 days under...

Page 23: ...nt controller The following steps outline the procedure for setting up communication For further instructions refer to the clinician s programming manual 1 Place the magnet perpendicular to and center...

Page 24: ...G is ready to pair with the clinician programmer or patient controller NOTE The EPG indicator light flashes faster when it is ready to pair than when batteries are inserted or a communication session...

Page 25: ...Figure 6 Magnet and keeper bar 1 Magnet 1 2 Keeper bar 2 2 Hold the magnet perpendicular to and centered directly over the EPG for 2 seconds 2 Figure 7 Holding the magnet over the EPG 19...

Page 26: ...the programmer and controller to ensure it is functional Refer to Setting Up Communication Between the EPG and the Clinician Programmer or Patient Controller page 17 for instructions CAUTION Before th...

Page 27: ...ader cap to expose the EPG stimulator port 1 2 Carefully slide the connector end of the multilead trial cable into the EPG stimulator port 2 CAUTION The EPG is not sterile When connecting and testing...

Page 28: ...ect the multilead trial cable from the EPG NOTE For further instructions refer to the clinician s manual for the multilead trial cable 1 Turn off stimulation on the EPG using the clinician programmer...

Page 29: ...ation outlines the suggested procedure for securing the leads or extensions to the patient Secure the leads or extensions and bandage the lead entry site For further instructions refer to the clinicia...

Page 30: ...the EPG header into the EPG body until it clicks into place Figure 9 Connecting the EPG header to the EPG Connecting the Leads or Extensions to the EPG Header To connect a lead or extension to the EPG...

Page 31: ...er comes with open ports and attached port plugs Do not remove the port plugs from the header If only using one lead or extension use the lower port labeled 1 8 and insert a port plug in the unused po...

Page 32: ...to lock the lead or extension into place 4 5 If applicable repeat the previous steps to insert the remaining lead or extension Do not disturb the 5 already inserted lead or extension Securing the EPG...

Page 33: ...e patient 5 Use additional medical tape to secure the pouch and leads or extensions further as needed 5 Programming the EPG Use the clinician programmer app to program the system for the trial period...

Page 34: ...not wipe over the stimulator port Do not submerge the EPG in fluid or use a cloth that is soaking wet Never use ammonia acidic or alkaline cleaners or organic chemicals such as paint thinner acetone p...

Page 35: ...At the end of a trial disable stimulation clean the EPG and attach the header cap before storing the EPG NOTE During a trial store the header cap for reuse Figure 11 EPG header cap 29...

Page 36: ...nformation 1 855 478 5833 toll free within North America 1 651 756 5833 For additional assistance call your local Abbott Medical representative Ordering Information To order parts contact Technical Su...

Page 37: ...1216 EPG header cap 1213 Pouch with adhesive 5 1214 Pouch without adhesive and belt 5 1218 Carrying case Appendix A Product Specifications EPG with Header The EPG Model 3599 and EPG header Model 3032...

Page 38: ...Nonrechargeable CR2450 coin cell Lead or extension compatibility 2 Octrode leads Expected service life 5 years Storage temperature 25 C 70 C 13 F 158 F Operating temperature 5 C 40 C 41 F 104 F Stora...

Page 39: ...frequency 10 60 Hz 10 Hz Intra Burst frequency 250 500 Hz 500 1000 Hz 10 Hz 20 Hz Amplitude 0 25 5 mA 0 1 1 0 mA 0 12 75 mA 0 05 0 50 mA Stimulation output Constant current Constant current NOTE Colu...

Page 40: ...and if not installed and used in accordance with the instructions may cause harmful interference to radio communications However there is no guarantee that interference will not occur in a particular...

Page 41: ...he following two conditions 1 this device may not cause interference and 2 this device must accept any interference including interference that may cause undesired operation of the device Statement of...

Page 42: ...in the domestic environment Wireless Technology Information The following table summarizes the technical details of the Bluetooth Low Energy LE wireless technology as it is implemented in the device T...

Page 43: ...2 MHz per channel Data rate 1 Mbit s Data flow Bi directional Protocol Bluetooth LE wireless technology EIRP Equivalent isotropically radiated power Radio Transmitter Cables Transducers The device co...

Page 44: ...and the clinician programmer or patient controller The requirements for the quality of service QoS vary depending on the use environment operating room recovery room and home environment After the cl...

Page 45: ...ommunicate with the generator at the same time A unique key for each unit that is checked during each transmission Built in pairing that specifies valid and legitimate pairing among units Proprietary...

Page 46: ...device Appendix C Electromagnetic Compatibility Guidelines The EPG hereafter the device is medical equipment and should be used with the following guidance The device requires special precautions with...

Page 47: ...are not approved by Abbott Medical Table 7 Guidance and Manufacturer s Declaration Electromagnetic Emissions Emissions Test Compliance Electromagnetic Environment Guidance RF emissions CISPR 11 Group...

Page 48: ...tery powered devices Voltage dips short interruptions IEC 61000 4 11 5 UT 40 UT 70 UT Not applicable No guidance for battery powered devices Power frequency 50 60 Hz magnetic field IEC 61000 4 8 30 A...

Page 49: ...rding to the maximum output power of the communications equipment Recommended minimum separation distance for higher immunity test levels where P is the maximum power in watts W d is the recommended s...

Page 50: ...dulation 27 V m Recommended minimum separation distance d 0 3 m 450 MHz 28 V m FM modulation 28 V m 710 MHz 745 MHz 780 MHz 9 V m 217 Hz pulse modulation 9 V m 810 MHz 870 MHz 930 MHz 28 V m 18 Hz pul...

Page 51: ...low the limits as specified in USA FCC 47 CFR Part 15 2012 Canada RSS 210 Issue 8 Europe ETSI EN 301 489 1 V2 2 0 2017 03 and ETSI EN 301 489 17 V3 2 0 2017 03 NOTE Maintain a reasonable distance betw...

Page 52: ...ct or product label For harmonized symbols refer to the Universal Symbols Glossary at medical abbott manuals Table 10 Symbols and definitions Symbol Definition Caution Refer to instruction manual book...

Page 53: ...other persons within an MR environment Non ionizing electromagnetic radiation Keep dry keep away from rain Do not re use Ingress protection rating for a device that is protected from the intrusion of...

Page 54: ...Table 10 Symbols and definitions Symbol Definition Use by date Date of manufacture Manufacturing facility Temperature limit Humidity limitation Atmospheric pressure limitation 48...

Page 55: ...finitions Symbol Definition Do not use if package is damaged Catalog number NOTE This symbol also refers to the model number Manufacturer Packaging unit Implantable device Accessories Prescription use...

Page 56: ...inappropriate waste handling of this product The recycling of materials will help to conserve natural resources For more information about how to return this product for recycling please contact Abbo...

Page 57: ...ott euconformity This device is listed by Nationally Recognized Testing Laboratory NRTL as certified Australian Communications and Media Authority ACMA and New Zealand Radio Spectrum Management RSM Re...

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Page 60: ...2023 02 ARTEN600279452 A 600279452...

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