Wat Medical Enterprise OE-M600 Wristband ObeEnd User Manual
- June 6, 2024
- Wat Medical Enterprise
Table of Contents
ObeEnd
[Name of Product]
Wristband-ObeEnd
[Specification and Model]
OE-M600
[Adverse Reactions]
If you experience adverse reactions, stop using the device and consult with
your physician. Users with sensitive skin may experience skin irritation in
the area where ObeEnd is applied.
[Warnings] DO NOT USE THIS DEVICE:
-
If you have a cardiac pacemaker, implanted defibrillator, or other implanted metallic or electronic devices.
Doing so could cause electric shock, burns, electrical interference or death. -
If you have epilepsy or a history of seizures.
-
If you have acute inflammation, or hemorrhagic tendency, or arrhythmia.
-
While during any activity in which electrical stimulation can put you at risk for injury.
-
While in a shower, bath, pool, or other body of water.
-
Over open wounds, sores or rashes, or over swollen, red, infected, or inflamed areas or skin eruptions. If you experience an adverse reaction, discontinue use.
-
In the presence of strong electromagnetic fields.
-
On children under the age of 18.
[Precautions]
- Use with caution if ObeEnd is placed over areas of skin that lack normal sensation.
- Clean the area of skin on which ObeEnd will be applied to.
- Use of accessories not approved by the manufacturer may cause harm or injury.
- Do not disassemble the device.
- ObeEnd should only be applied on normal, intact, healthy skin as instructed.
- Operation in close proximity to short wave or microwave therapy equipment may produce instability in the device output.
- Keep the device out of reach of children.
[Limited Warranty]
If you purchase ObeEnd and you are not completely satisfied with the product
for any reason within 30 days of purchase, we would refund your purchase
price, excluding taxes and shipping charges.
[Environmental and Technical]
| Power Supply | 3.7V DC. 140mAh Lithium battery |
|---|---|
| Waveform | AC sharp-wave |
[Operating Conditions]
Normal operating conditions should comply with the following requirements:
Environment temperature: 5∼40ºC
Relative humidity: 10∼80%
Atmospheric pressure: 86∼106kPa
[Storage]
The product should be stored in accordance with the following requirements:
Environment temperature: -20∼55ºC
Relative humidity: 10∼80%
Atmospheric pressure: 50∼106kPa
Indoor, dry and well-ventilated, free from corrosive substances Great pressure
is not allowed to be put on the product.
DO NOT PLACE THE DEVICE:
- Across your chest. The introduction of an electrical current to the chest may cause rhythm disturbances to your heart, which could be lethal.
- On any part of the body other than those instructed.
- Over the carotid sinus nerves, the front of the neck, or around the mouth.
[Disclaimer]
- The device ObeEnd has not been evaluated by the Food and Drug Administration. This device is not intended to treat, cure, or diagnose any diseases or medical conditions.
- Please note that ObeEnd is intended solely for use by healthy adults only for purposes of reducing weight. We hope to expand the use of this technology to help people with specific medical conditions in the future, but we have not yet gathered the clinical data necessary to advise on the safety or efficacy of the use of ObeEnd for any such purposes.
- The device ObeEnd is not recommended for use by individuals who are under the age of 18; have implanted metal or electronic medical devices in the head or neck; have a cardiac pacemaker or implantable cardioverter-defibrillator; have a history of seizures. Consult your physician if you believe any of these may apply to you, or if you have any other concerns.
[Manufacturing Enterprise and After-sale]
Manufacturer: NeuWave Medical Inc.
Add.: No.66 Wanyuan Road, Dianshanhu Town, Kunshan City, Jiangsu Province,
China
Email: info@neuwavetechnology.com
FCC Statement
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.
Changes or modifications not expressly approved by the party responsible for
compliance could void the user’s authority to operate the equipment.
NOTE: 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 by turning the equipment off and
on, the user is encouraged to try to correct the interference by one or more
of the following measures:
- Reorient or relocate the receiving antenna.
- Increase the separation between the equipment and receiver.
- Connect the equipment into an outlet on a circuit different from that to which the receiver is connected.
- Consult the dealer or an experienced radio/TV technician for help.
The device has been evaluated to meet general RF exposure requirement. The device can be used in portable exposure condition without restriction.