User's Manual for additional information on this capability.
Somnibel Pro
has been designed for being used by a physician or a technician trained in SRBD and SAHS. The
user is allowed to configure the device under these conditions. However, it is not recommended to prescribe the
treatment with the device or change the treatment settings without a previous understanding of the physiologic
principles of positional therapy for patients with SAHS. Contact
Somnibel Pro
is indicated for patients older than 18 years, weighing over 40 kg and a height over 145 cm. Medical
personnel should inform the patient about the device use, its cleaning and the required precautions described
in section WARNINGS, before prescribing the positional therapy with the
Somnibel Pro
uses a rechargeable Lithium-polymer battery and includes USB connection for battery charge and
transmission of recorded data to a personal computer. It is recommended to fully charge the battery before the
first use of the device.
Somnibel Pro
must be adhered to the patient's body, at the forehead or chest, by means of a specifically designed
disposable fastening adhesive. The fastening adhesive should not be placed onto injured skin. The patient should
adopt a lying sleeping position (trunk inclination < 30º) while using the device.
Somnibel Pro
Although
SPECIFICATIONS), it is recommended to sleep with a room temperature between 18ºC and 26 ºC. A hot
environment may induce excessive sweating that can deteriorate the adherence of the adhesive.
Somnibel Pro
is conceived for being used at the patient's home and, occasionally, in a health center. The device
can be used by different patients after performing the required cleaning between each patient.
The use of the device in an environment with vibrations, such as moving transport vehicles (car, train, airplane,
etc.) may modify its functioning.
534-80P-MUM_Rev.1.08
can be used within conventional environmental conditions (see section TECHNICAL
somnibel Pro
SIBEL S.A.U.
for additional training.
Somnibel Pro
User's Manual
device to the patient.
EN 6