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China, Chinese Professional Pharmaceutical Factory Isolated Washer Extractor 100kgs1 Industrial Products Supplier Manufacturer Details, price list catalog:
China Industrial Products Supplier Manufacturer List Catalog
Washing EquipmentIndustrial Laundry DryerWashing MachineBarrier Washing Machine
Jiangsu Sunflower Machinery Co., Ltd.
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Product Description Professional Pharmaceutical Factory Isolated Washer Extractor 100kgsModel BW100Inner Drum (mm)Φ 1200×890Motor Power (kw)11Washing Speed (rpm)32Rotation (rpm)65Extracting Rotation (rpm)350Fast Speed Rotation (rpm)750Steam Inlet (mm)DN25Water Inlet (mm)DN50Drain (mm)Φ 140Water Pressure (Mpa)0.2-0.3Steam Pressure (Mpa)0.4-0.6Air compressor (Mpa00.4-0.5Water Consumption (kg)1650Steam Consumption (kg)50Electricity Heating Power (Kw)48Overall Dimension (mm)1720*1810*2150Weight (kg)3000 charactersBarrier Washing Extractor machines are widely used in laundry shops, hospitals and pharmaceutical factories.This machine has Two way opening, separate opening for dirty and clean side of washing machine ,The dirty clothes will be put into the washer extractor at one side of the barrier washer extractor and the washed and disinfectant clothes will be unloaded from the clean room to avoid cross infection.1.1 Additional FeaturesAll metallic non cloth contact surfaces should be constructed of stainless steel AISI 304 / 1.4301 or higher quality with external surface finish < 1.2 μm Ra, matt finishInternal finish of drum: polished (vendor to submit details)Sealing material and non-metal parts for elements having contact with product: Food Grade with FDA certificate Vendor to ensure all pipe connections are as per latest ASME BPE / ISPE standards T/C nozzles and sanitary fittings External doors with verticals hinges and easy to handle, reversible Automatic drum positioning and locking for the loading and unloading operationLarge door opening for easy loading and unloadingEnergy saving designPower balance that ensures the best extraction whatever the loading condition areConstant airflow over time for a process always under control4 compartment soap box to use liquid or powder and detergentsStatic prevention systemControl-panel, showing all the process relevant parameters Control panel will be featured with the following: Programming buttonsOptical interface for PCMulti-function selector with turn and press mechanismCycle complete lamp for status indication Wash cycle running LAMP for status indication Emergency Stop SwitchIntegrated weighing system to optimise the loading operationsWater inlet valve shall be providedAll conditions of important actuators, drives, operational situations, safety equipment and similar items, must be monitored1.2 Safety Features Emergency stop function on accessible areasAppropriate closure on all rotating partsAppropriate failure detection and alarm notificationOn power failure equipment must come to rest to protect operator and equipment itself and the cloth must remain protected from any kind of product quality degradationPower restart must not be automatic and human intervention must be requiredThe electrical system of the equipment shall be housed as per the cGMP and cGEPMachine shall consist of emergency button and control ON/OFF switch1.3 Material of ConstructionAll metallic non cloth contact surfaces should be constructed of stainless steel AISI 304 / 1.4301 or higher quality with external surface finish < 1.2 μm Ra, matt finishInternal finish of drum: polished (vendor to submit details)Sealing material and non-metal parts for elements having contact with product: Food Grade with FDA certificate Vendor to ensure all pipe connections are as per latest ASME BPE / ISPE standards T/C nozzles and sanitary fittingsThe complete hardware and software systems shall comply with the current requirements for the use of computerized systems in the pharmaceutical industry, especially the requirements of 1.4 General ConditionsAnnex 11: computerized systems (revision January 2011), EC guide to good manufacturing practice for pharmaceutical products (EC-GMP Guideline- cGMP)GAMP 5FDA 21 CFR Part 11 (Validated Software)1.5 Access Regulations / User AdministrationUser-administration (i.e. password issue) is to be carried out by the IT- administratorAccess to the equipment controls shall be restricted by means of passwordEthernet / Modem for the remote access for the service1.6 System Reliability and MeasuresThe system is designed according to the environmental conditions and process requirements so that, even under full-load and continual-operation, the required performance capability is always guaranteed. Should there be a system breakdown, the re-establishment of the previous state must be possible, if necessary by using the backup copies.1.7 Quality Control MeasuresFor the software development, the contractor must present a quality management with test environment and test tools, which is to be auditedThe standard modules and whichever adaptations are required must be descriptively presentedFor the operation, the system and operator handbooks must be supplied in English including fault correction procedures. Maintenance procedures and intervals must be stipulated. All necessary procedures for data protection / backups, user administration, system recovery and routines for fault analysis / rectification, are to be documented in the manualsThe source code must be permanently stored by the supplierThe processing of data (process sequences, algorithms, interlocks, supervision, and alarms, fault processing, logging, plausibility check) shall be undertakenSafe, easily directed menu guided interface for the userUser friendly structured operation of the control interface (clarity, logical format, ergonomic layout), to rule out errors being caused by incorrect operationDiagrammatic display of parameter values (trend curve)Input and output-data are to be displayed in suitable form, so that the operator can enter data quickly and easily (monitor, keyboard, mouse, or similar)An appropriate procedure is to be planned for the storage of process-data, so that the data can be deposited on the operating computers hard-disk, using clear file names1.8 Data ProcessingThe processing of data (process sequences, algorithms, interlocks, supervision, and alarms, fault processing, logging, plausibility check) shall be undertakenSafe, easily directed menu guided interface for the userUser friendly structured operation of the control interface (clarity, logical format, ergonomic layout), to rule out errors being caused by incorrect operationDiagrammatic display of parameter values (trend curve)Input and output-data are to be displayed in suitable form, so that the operator can enter data quickly and easily (monitor, keyboard, mouse, or similar)An appropriate procedure is to be planned for the storage of process-data, so that the data can be deposited on the operating computers hard-disk, using clear file namesSensors for process relevant parameters must be calibrated. Suitable adjustment possibilities are to be plannedWashing cycle report shall be available for print with start /end including stage cycle1.9 PrintoutsTotal cycle time Trend curvesDetergent and softening agent quantity usedUS FDA 21 CFR part 11 compliance printout Photos of Professional Pharmaceutical Factory Isolated Washer Extractor 100kgsCertificate of Professional Pharmaceutical Factory Isolated Washer Extractor 100kgs
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