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Technical sheet

TÜV CERTIFIED* AND HEALTH CANADA cleared medical device

Universal Power Supply:

120/230 V~ 60/50 Hz

Fuse Type:

T1.5 AL (120/230 V~)

Applied Parts Degree of Protection:

Type BF

Operating Mode:

Continuous

Current Consumption:

1.0 A

Protection Class:

1 (Grounded)

Tolerance / Accuracy of display:

± 15 %

Acoustic Output Frequency:

3 MHz continuous sine wave

Maximum Acoustic Output Power:

4.32 W

Maximum Acoustic Power Density:

0.35 W/ cm

Effective Radiating Area:

12.5 cm

BNR:

0.07

Beam Type:

Divergent

Water-ingress Rating:

IPX7

Maximum HVPC Signal Amplitude:

135 V p-p

HVPC Signal Durations:

60-90-120 µs

Maximum Micro Currents:

3000 µA

Micro Currents Carrier Frequency:

187.5 Hz

Unit Dimensions:

Width: 15 in (381 mm)
Height: 9 in (229 mm)
Depth: 21 in (535 mm)

Unit Weight:

10 lb (4,5 kg)

Equipment Construction:

Internal steel frame
Kydex body

Electronics:

Microprocessor controlled

Hand-held Accessories:

Piezoelectric actuator

Ambient Operating Temperature:

+10°C to +40°C

Ambient Operating Humidity:

30% to 75% HR

Ambient Operating Atmospheric Pressure:

700 hPa to 1060 hPa

(*) Tested to comply to the applicable standards and equipment specifications: IEC 60601-1-2:2007-(Ed3.0) ICES-003 Issue 4:2004 / FCC Part 15 Subpart B 15:2010 IEC 60601-1-2:2007-(Ed 3.0) Group 1, Class A CAN/CSA C22.2 CAN/CSA C22.2 No. 60601-1:2008 excluding Biocompatibility (clause 11.7), Usability (clauses 7.1.1, and 12.2), PEMS (clause 14), and EMC clauses 7.9.2.2 and 17). CAN/CSA C22.2 No. 60601-2-5:2011 excluding EMC (clause 17) UL 60601-1:2003 excluding EMC (Clauses 6.8.2, and 36), Biocompatibility (Clause 48), and PEMS (clause 52.1 as it pertains to IEC 60601-1-4). IEC 60601-2-5:2000 excluding EMC (clause 36) ANSI/AAMI ES 60601-1/A2:2010 excluding Biocompatibility (clause 11.7), Usability (clauses 7.1.1, and 12.2), PEMS (clause 14), and EMC (clauses 7.9.2.2 and 17). IEC 60601-2-5:2009 excluding EMC (clause 17)