24967 Patient Connector Technical Manual Caution: Federal law (USA) restricts this device to sale by or on the order of a physician.
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Contents 1 Introduction to the 24967 Patient Connector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.1 Explanation of packaging and product symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.2 Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
1 Introduction to the 24967 Patient Connector 1.1 Explanation of packaging and product symbols Refer to the package label and product to see which symbols apply to this product. Consult instructions for use at www.medtronic.com/manuals. Conformité Européenne (European Conformity). This symbol means that the device fully complies with applicable European Union Acts.
Re-order number Serial number Package contents Product documentation Accessories Magnetic Resonance (MR) Unsafe Bluetooth connection Wireless communication enabled Telemetry enabled Caution: Strong magnet Follow instructions for use (blue) Low battery Keep dry ACMA (Australian Communications and Media Authority) and the New Zealand Ministry of Economic Development Radio Spectrum Management compliance mark for Australia and New Zealand System meets the applicable Canadian and U.S.
Transit temperature Storage temperature Security key 24970A Device manager 24967 Patient connector 249701 Power supply (for the 24970A base) 249705 Power cord (for the 24970A base) 249651 Power supply (for the 24967 patient connector) 249672 Tether Kit 249702 USB Cable 249671 Weight Kit 1.
1.4 Contraindications There are no known contraindications for the use of this device. 1.5 Warnings These warnings apply in general to using the patient connector settings. For more information related to specific implantable device models, see the reference guides for the implantable device and the software. Battery exposure – Exposing the patient connector to cold temperatures may result in a loss of performance and shortened patient connector service life.
If the patient connector does cause harmful interference to other devices or is negatively impacted by other devices, correct the interference by one or more of the following measures: • Reorient or relocate the patient connector and other devices. • Increase the separation between the patient connector and other devices by at least 2 m (approximately 6 feet). Other devices include, but are not limited to, cellular phones, computer screens, wireless network devices, and ‘walkie-talkies’.
To use the Medtronic app, you must also enable Bluetooth wireless technology on your mobile device. The patient connector communicates with the Medtronic app installed on the mobile device through a Bluetooth connection. Failure to provide Bluetooth wireless communication access prevents the patient connector from communicating with the Medtronic app. If Bluetooth connectivity is disabled, the patient connector cannot interrogate, analyze or program Medtronic implantable devices.
2 Setup and configuration 2.1 Contents of package The package contains: • • • • Model 24967 Patient Connector MENB1020A0500XXX Power Supply (Medtronic re-order number: 249651) Model 249652 Tether Kit Literature 2.2 System components Figure 1. Patient connector components 1 Weight (blue) 2 Patient connector 3 Tether kit 4 Power supply Patient connector – Provides the communication link between the app and the patient’s implantable device.
2.2.1 Indicator lights Figure 2. Patient connector indicator lights 1 Telemetry status 2 Bluetooth connection status Table 1. Patient connector icons and indicator lights Icon Indicator Telemetry status Bluetooth connection status Battery status 3 Battery status Color Amber State Solid Green Solid Blue Flashing Blue Solid Amber Green Solid Flashing Green Solid Description The patient connector is out of range of the implanted device.
2.4 Setup This section describes how to: • • • • Power on the patient connector Power off the patient connector Download the app Attach the optional tether kit 2.4.1 Powering on the patient connector 1. Locate the button on top of the patient connector. Figure 3. Locate the patient connector button 1 Patient Connector button 2. To power on the patient connector, press and release the button. The Bluetooth connection status light flashes when the patient connector is turned on. 2.4.
3. Remove the power supply cover from the patient connector. 4. Plug the power supply into the patient connector. 5. Slide the cable retainer over the power supply plug of the power cord. 6. Insert the screw into the bottom of the cable retainer and tighten the screw using the Medtronic-supplied wrench. Caution: Do not over tighten the screw when attaching the tether kit. Warning: Use the Medtronic-supplied components only.
1. Open the power supply connector cover located on the bottom edge of the patient connector. 2. Connect the power supply cord to the patient connector. 3. Plug the power supply into the AC power outlet (AC mains). Warning: Use only the Medtronic-supplied power supply to power the patient connector. Use of an unapproved power supply may damage equipment or impact user or patient safety. 2.
7. Locate the security key code on the back of the patient connector. Figure 4. Patient Connector security key 1 Security key symbol 2 Security key code 8. Enter the security key code and follow the instructions in the app to continue. 9. Accept the Bluetooth pairing request on the mobile device. 10. Complete the configuration steps in the app. 2.7 Troubleshooting potential interference Interference between the patient connector and other electronic equipment can result in reduced quality of service.
1. Tap the app icon to open it. 2. If the patient connector isn’t already on, turn on the patient connector by pressing the button. 3. Place the patient connector over the implantable device. The telemetry status light on the patient connector is green when communication is established with the implantable device. The telemetry status light is brighter when there is a stronger signal. 4. Follow the instructions in the app to start communicating with the implantable device. 5.
Condition Action Result that nothing physical is blocking the signal between the patient connector and the mobile device. 4 Maintaining the patient connector 4.1 Cleaning and disinfecting the 24967 patient connector 4.1.1 Cautions and notes for cleaning and disinfecting Cautions: • Clean and disinfect the patient connector as needed according to your organization’s policies. Use only the recommended methods to clean and disinfect the patient connector.
3. Unwrap the blue weight from around the patient connector and fully extend the cord. 4.1.3 Cleaning the patient connector 1. Clean the patient connector thoroughly using one of the following cleaning methods: • A 70% isopropyl alcohol prep pad. • A sterile gauze pad or sponge dampened with 70% isopropyl alcohol. 2. Wipe all external surfaces of the patient connector to remove all visible soil. a. Wipe the blue weight and its cord. b.
e. If the optional tether kit is installed to secure the power supply cord or USB cable, wipe the cord or cable for approximately 1 m (3 feet) extending from the patient connector. 3. Allow to air dry approximately 5 minutes or until dry. Leave the blue weight fully extended until it is dry. 4.1.4 Disinfecting the patient connector 1. Follow the steps in the previous section to thoroughly clean all external surfaces of the patient connector.
b. Wrap all sides of the patient connector to completely cover it. 5. To maintain a wet or damp exposure time of 15 minutes and reduce evaporation, place all wrapped components of the patient connector inside a plastic bag or container. Seal the bag or container to reduce evaporation. 6. After 15 minutes have elapsed, remove all wrapped components of the patient connector from the plastic bag or container. 7.
4.1.5 Reassembling the patient connector 1. Rewrap the blue weight around the patient connector and secure it in the top of the retention channel. 2. Install a new replacement tether kit with a new USB cable or power supply, if needed. This is an optional configuration. 4.1.6 Additional resources For additional information about cleaning and disinfecting the patient connector, contact Medtronic Instruments Technical Services: • Phone: +1 800 638 1991 • Email: tshelp@Medtronic.
3. Unwrap the blue weight from around the patient connector and fully extend the cord. 4. Remove the nose, the cable, and the weight. 5. Thread the cable with the weight through the hole in the nose. 6. Place the new nose on the patient connector and line up the screw hole.
7. Wrap the blue weight around the patient connector and insert the screw into the screw hole. Use the Medtronic-supplied wrench to tighten it. 4.3 Software updates Software updates will be pushed automatically to the patient connector when you start a communication session in the app. Updates can take up to 5 minutes. You must wait until the update is complete before you can continue with the session. 4.4 Specifications Table 2.
Table 2. Patient connector specifications (continued) Physical dimension and weight Length 16.7 cm (6.6 in) Width 7.3 cm (2.9 in) Depth 3.0 cm (1.2 in) Weight 0.25 kg (0.
Guidance and manufacturer’s declaration—electromagnetic emissions The 24967 patient connector is intended for use in the electromagnetic environment specified below. The customer or the user of the 24967 patient connector should assure that it is used in such an environment. Emissions test Compliance Electromagnetic environment—guidance RF emissions Group 1 The 24967 patient connector uses RF energy only for its internal funcCISPR 11 tion.
Guidance and manufacturer’s declaration—electromagnetic immunity The 24967 patient connector is intended for use in the electromagnetic environment specified below. The customer or the user of the 24967 patient connectorshould assure that it is used in such an environment.
Recommended separation distances between portable and mobile RF communications equipment and the 24970A base Note 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies. Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects, and people.
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