SA-232
SA-232 | ||
---|---|---|
腔室容積 | 16 L | 4.2 gal |
腔室尺寸 | Ø 230 x 410 mm | Ø 9.1 x 16.1 in |
外觀尺寸 (W x H x D) | 335 x 430 x 510 mm | 13.2 x 17.0 x 20.1 in |
淨重 | 15.5 kg | 34.2 lb |
毛重 | 20 kg | 44.1 lb |
電壓 / 頻率 / 功率 | 110 V / 50-60 Hz / 1,200 W 230 V / 50-60 Hz / 1,400 W |
|
海拔限制 | Under 1,000 m | |
空氣移除 | Gravity |
ISO 13485:2016 Quality Management System - Medical Devices
93/42/EEC Medical Device Directive
PED 2014/68/EU Pressure Equipment Directive
EN/IEC 61010-1 Safety Requirements for measurement control and laboratory use
EN/IEC 61010-2-040 Safety requirements for sterilizers used to treat medical materials
EN/IEC 61326-1 for EMC Requirements for electrical software
RoHS Restriction of Hazardous Substances Directive 2011/65/EU
SA-232 | ||
---|---|---|
腔室容積 | 16 L | 4.2 gal |
腔室尺寸 | Ø 230 x 410 mm | Ø 9.1 x 16.1 in |
外觀尺寸 (W x H x D) | 335 x 430 x 510 mm | 13.2 x 17.0 x 20.1 in |
淨重 | 15.5 kg | 34.2 lb |
毛重 | 20 kg | 44.1 lb |
電壓 / 頻率 / 功率 | 110 V / 50-60 Hz / 1,200 W 230 V / 50-60 Hz / 1,400 W |
|
海拔限制 | Under 1,000 m | |
空氣移除 | Gravity |
ISO 13485:2016 Quality Management System - Medical Devices
93/42/EEC Medical Device Directive
PED 2014/68/EU Pressure Equipment Directive
EN/IEC 61010-1 Safety Requirements for measurement control and laboratory use
EN/IEC 61010-2-040 Safety requirements for sterilizers used to treat medical materials
EN/IEC 61326-1 for EMC Requirements for electrical software
RoHS Restriction of Hazardous Substances Directive 2011/65/EU