Technical Device Data
General Data:
Brand, Model: BTL EMSELLA
Technical Device Type: Medical Device - Electromagnetic
Serial Number: 09900B003008
Year of Manufacture: 2020
Mileage: Unknown
Manufacturer: BTL Industries Ltd
Technical data of the valuation item:
Parameter Value / Notes
11.2 BTL Seat Applicator — Identification
Name BTL Seat Applicator
Operating Conditions
Ambient Temperature +10°C to +30°C
Relative Humidity 30% to 75%, non-condensing
Atmospheric Pressure 700 hPa to 1060 hPa
Position Vertical
Seat Positioning System Operation Type
Max. ~119 min (continuous operation time: 1 minute)
Transport and Storage Conditions
Ambient Temperature −10°C to +55°C
Relative Humidity 10% to 95%, non-condensing
Atmospheric Pressure 650 hPa to 1100 hPa
Position Vertical
Power Supply and Safety
Maximum Input Power 80 W
Power supply voltage 100 to 240 V AC
Frequency 50 to 60 Hz
Protection class (IEC 60601-1) I
Disconnection from the mains By the power cable
Patient side part type BF, designed for a single patient
Essential function according to the standard IE C60601-1
No essential function
Design/dimensions
Maximum working load (patient)
150 kg (330 lb)
Seat height adjustment range
(±20%) 420 mm (16.5 in) to 665 mm (26.2 in)
Dimensions (W × H × D) - chair approx. 730 × 730 × 750 mm (29 × 29 × 29 in)
Package dimensions (W × H × D) approx. 800 × 890 × 800 mm (31 × 35 × 31 in)
Accessories:
- BTL-299-3 armchair applicator, serial number 29930B000438, manufactured in 2018, with remote control,
- User's manual,
- Power cord x 2
How it works
The device consists of a control unit and a chair-shaped applicator.
The chair seat contains an electromagnetic coil that generates a high-energy electromagnetic field with an induction of up to 2.5 Tesla during the treatment. This field penetrates the patient's clothing and reaches the pelvic floor muscles, causing intense, repetitive contractions.
During a single session, thousands of such contractions occur, the intensity and frequency of which exceed the capabilities of voluntary muscle effort.
The stimulation results in strengthening and remodeling of the muscle structure, improving muscle tone and endurance, and consequently, increasing bladder control and improving the quality of life for patients.
The device is completely non-invasive – the patient remains clothed, and there is no need for conductive gels or probes. The therapy does not require a recovery period, and the patient can return to daily activities immediately after the treatment. Technical Condition Description
Nameplate:
- Location – rear housing,
- Tampering/irregularities – none.
Identification Number Stamped:
- Location – not located.
Technical Documentation:
- User Manual – yes, in Polish,
- Parts Catalog – none,
- Technical Specifications – no.
- Device Technical Passport – none.
CE/EC Certificate:
- Marking – yes,
- Declaration/Certificate of Conformity – none.
Operation History:
- Service Documentation – none,
- Periodic Inspection Markings – yes – next inspection due June 2026.
Year of Manufacture:
- 2020 – determined based on the permanently affixed markings on the nameplate. Technical condition:
- Visual appearance – good, the device requires thorough cleaning, minor scratches found on the device's casing.
- Wear – undetermined – no operating time counter, device wear considered normal.
- Operating system – the device is connected to a power source, starts up correctly, menu navigation is flawless, treatment has been initiated, the device does not report any errors, the device has not been tested with a patient.
- Central unit (device) – panel – scratches and signs of use, screen – minor scratches.
- Seat (applicator) – local scratches and abrasions on the edges of the base, side plastic panels – minor surface scratches, upholstery – no tears,
in good condition, with some soiling and spot damage.
- Other – no information on the operation and service history. |
