SONICA 60L EP

Ultrasonic Cleaning is a safe and efficient modern procedure, which ensures perfect cleaning within the shortest time possible. It has many advantages over ordinary cleaning methods.Ultrasonics can remove even the most tenacious deposits from parts which would be difficult to reach by hand, it also reduces the risk of injury or infection which may occur during manual cleaning.

General characteristics

60 Litres

Product Code:090.003.0039

Serie:60L EP

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SONICA 60L EP

230/240 V~50/60Hz700 W

2200 W1400 W

40 khz ± 5%1/2”

166030

Class II acording to EN 61010Temperature Rel. Hum. 80% up to 31°C with linear decrease up to 50% at 40°C

SOLTEC S.r.l. Via Castelbarco, 17 - 20136 MilanoTel. +39 0258308378 - Fax +39 0258308595

www.soltec.it - e.mail: info@soltec.it

1160 mm360 mm425 mm

1100 mm300 mm200 mm

CERTIFICATO N° 04100041419(DIN EN) ISO 9001:2008

300 mm 1100 mm

200mm

1160 mm

425mm

360 mm

EP

Steel AISI 304Steel AISI 316Ti

20/10

Technical DataMain line voltageMain input power/consumptionMain input power with heatingPeak HF ultrasound power US fequency Liquid drain Transducers Tank capacityWeight (Kg)Installation categoryEnvironmental conditions

Constructive Materials

External DimensionsTank DimensionsLength Breadth Height

Length Breadth Depth

60 Litres

Available series

Serie EP The most technologi-cally advanced of the SONICA range: Sweep System genera-tor; modern digital display control panel windows; degas time setting;cleaning times from 0 to 99 minutes; tank liquid temperature setting up to 70°C; memory for 9 cleaning program-mes; jet program function to start quickly and easily cleaning cycle.

Housing Tank

Notes for use as “Medical Devices”:

Denomination: Ultrasonic Cleaning DeviceUMDNS-nomenclature (ECRI) 14-263Field of application: cleaning and disinfection of surgical and dental instrumentsClassification (Medical Devices Directive 93/42/EEC, appendix IX):Class I, Non Active MD, Non Invasive MD, Non Implantable MD 2004/108/EC EMC Directive (EN 61326)

2006/95/EC LV Directive (EN 61010-1)2007/47/EC Medical Device Directive

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