| Theory: | Pressure Steam |
|---|---|
| Type: | Pressure Steam Sterilization Equipments |
| Certification: | CE, ISO13485 |
| Electric Tension: | 220V |
| LCD Display: | LED High Light |
| Ultra High Temperature Alarm: | Ultra High Temperature Alarm |
| Customization: |
|---|
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High Quality Class N table top Autoclave 18/23L LED display
| Sterilization Class | CLASS N |
| Sterilization Temperature | 121ºC &134ºC |
| Dry System | Heating drying system |
| Display | LED display |
| Control Precision | Temperature: 0.1ºC Pressure: 0.1bar |
| Safety System | Relief valve Hand lock door Pressure or temperature over load protection Alarm system |
| Tray Holder | 5 layers tray holder with 3 trays |
| Chamber | Medical stainless steel 304 Max working pressure:2.3bar Min working pressure: -0.9bar Max temperature: 145ºC |
| Operation Temperature | 5~40ºC |
| Noise | <50db |
| Water consumption in one cycle | 0.6L~0.8L |
| Color | Purple, Green, Grey, Tiffany, Blue |
| Program | Pressure | Sterilization Time | Drying Time |
| 134ºC | 210kPa | 6 min | 20 min |
| 121ºC | 110Kpa | 20 min | 20min |
| Model | Voltage/Power | Chamber Size | Packing Size | Net Weight |
| Z-COLOR 18 | 220V/1200W | Φ245×320mm | 660×525×495 | 25 |
| Z-COLOR 23 | 220V/1200W |
Φ245×450mm
|
770×530×495 | 30 |
| Directive or Standard No. | Directive or Standard Name |
| MDD 93/42/EEC | Medical Device Directive |
| PED 97/23/EC | Pressure Equipment Directive |
| EN 61010-1 | Safety regulations for electrical measuring, controlling and laboratory Devices- Part 1: General requirements |
| EN 61010-2-040: | Safety requirements for electrical equipment for measurement, control and laboratory use -Part 2-040: Particular requirements for sterilizers and washer-disinfectors used to treat medical materials |
| EN 13060 | Small steam sterilizers |
| EN 61326-1 | Electrical equipment for measurement, control and laboratory use - EMC requirements |
| Quality System No. | Quality System Name |
| ISO 9001 | Quality management systems-Requirements |
| ISO 13485 | Medical device-Quality management systems-Requirement for regulatory purposes |
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