MELA  uick®12+ p q The stand-alone device. Interfaces and   connections. This innovative device concept can also be used if there is no compressed air connection in the preparation room. MELA quick®12+ p has a compressor pump integrated into the device, which permits operation of the autoclave irrespective of location. The functionality and short operating times are identical in both MELA quick®12+ devices. Documentation and approval. Possibilities for documentation, batch release and re-tracing known from the Pro- and PremiumClass MELAG device series are also available for the MELA quick®12+. Starting with MELA flash through the MELA  net Box for network integration up to approval and marking of the instruments with MELA  soft ®. Device fuse —16 gRL Plug on the side for sterile filter (only in MELA quick®12+ p) Data and facts. Device fuse —10 AT Connection for monitoring the feed water container Air removal principle Fractionated gravity method Drying Pulsating overpressure drying Feed water Demineralized water, distilled water Device dimensions (Width x Height x Depth) 20.5 x 46 x 45 cm Connection for external waste water container Chamber (Ø x Depth) /  Volume 9 x 20 cm  / 1.35 l Weight (empty) approx. 23 kg Spring safety valve Operating overpressure / Operating temperature 2.2 bar  / 136 ºC Slit for emergency unlocking Electrical supply 220 – 240 V, 50 / 60 Hz, 10 A, 2050 W Connection for monitoring the waste water container Connection for compressed air (only in MELA quick®12+) Mains connection for IEC plug Connection for external feed water container MELA  uick®12+ / p is manufactured in line with the following directives and standards  q : 93 / 42 / EEC Medical devices, class IIb (European Directive for Medical Devices), 97/ 23 / EC (Pressure Equipment Directive), 2006 / 42 / EC (Machinery Directive)  EN 13060 (small steam sterilizers), EN 61010-1/-2-040 (safety requirements for ; electrical equipment for measurement, control and laboratory use — part 1 and part 2), EN 61326-1 (electrical equipment for measurement, control and laboratory use — EMC requirements — part 1: general requirements), EN 60601-1-2 (general requirements for safety including important performance characteristics — supplementary standard  electromagnetic : compatibility — requirements and tests), ISO 9001 and ISO 13485 (quality management /certification). Rev 0 -11/ 0572 .  03.11.5E -TB - MQ12+ Serial interface (RS232) for documentation You can find additional information on our homepage : www.melag.com MELAG Medical Technology Geneststraße 6 – 10 10829 Berlin MELA  uick®12+ q Compact. Fast.  Strong.

Operation  — no compromises. The requirement. Requirements for the preparation of dental instruments are defined by official hygiene experts. Instruments for “semicritical” use (restorative treatment) have to be prepared and treated after each patient, preferably in a validated, mechanised disinfection and cleaning process. If no mechanical prepa­ ation and treatment process is used, a manual process r can be selected, but it has to be concluded with sterilization of the instruments. “Critical” hand pieces and turbines used for paradontological, endodontic and surgical treatment have to be sterilized...