Medify TITAN-IR TD-01A Transcranial Infrared Therapy and Neuromodulation User Manual
- June 13, 2024
- Medify
Table of Contents
TITAN-IR TD-01A Transcranial Infrared Therapy and Neuromodulation
Product Information:
- Product Name: Medify PBM Device
- Manufacturer: Medify Inc.
- Website: https://www.medifypbm.com
- Date of Manufacture: [Not provided]
- IP Rating: IP22
- Compliance: FCC Part 15
- Age Restriction: Above 18 years
- Hazardous Substances: Complies with restriction
Product Usage Instructions:
-
Do not discharge the device during regular use.
-
Avoid using any other cleansing devices as they may cause
damage to the Medify PBM Device. -
To control the device, download the app from the manufacturer’s
website. -
Before first use, charge the device until it is fully charged.
The charging time may take a few hours. -
To charge the device, connect it to a power source using the
provided charging cable. -
After charging, disconnect the device from the power source and
start using it. -
Avoid using the device with other transcranial treatments such
as rTMS, TDCS, or ECT. -
If you experience any issues or have any questions, refer to
the manufacturer’s website for further support. -
The device can be used in portable exposure conditions without
restriction. -
Contact Information:
- Medify Inc.
- 90292 Marina del Rey
- California, USA
- Website: https://www.medifypbm.com
discharge during regular use.
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·
use any other cleansing Devices as these may damage the Device.
·
·
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device in the app.
· ·
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into the device. charging. full second.
charged.
device and charge the device. Charge the device.
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Team.
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other transcranial treatments such as rTMS, TDCS, or ECT. Researchers have deduced that there
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report.
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Date of Manufacture. 30
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40°C 0°C 30%
IP22
This symbol means: Conforms to certain EC Directives on health, safety, and
environmental protection standards. CE stands for”Conformité Européenne’. This
symbols implies conformity to UK Directives on health, safety and
environmental protection standards. UKCA stands for UK Conformity Assessed.
Handle the packaging with care
Restriction of hazardous substances.
This symbol indicates the device can be used whe age above 18.
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10. FCC Statement
void the user’s authority to operate the equipment. This equipment has been
tested and found to comply with the limits for a Class B digital device,
pursuant to Part 15 of the FCC Rules. These limits are designed to provide
reasonable protection against harmful interference in a residential
installation. This equipment generates uses and can radiate radio frequency
energy 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 installation. If
this equipment does cause harmful interference to radio or television
reception, which can be determined
· Reorient or relocate the receiving antenna. · Increase the separation
between the equipment and receiver.
connected.
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This device complies with part 15 of the FCC rules. Operation is subject to
the following two conditions (1)this device may not cause harmful
interference, and (2) this device must accept any interference received,
including interference that may cause undesired operation. The device has been
evaluat ed t o meet general RF exposure requirement .The device can be used
inport able exposure condit ion w it hout rest rict ion.
11. Contact Information
Medify Inc.
90292 Marina del Rey California, USA
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