Poseidon I GMP cleaning machine Introduction: Our pharmaceutical industry and life science industry cleaning system is used to clean key components, such as fermentation tank, atmospheric sphere bottle, large glass products, filling and packaging machine parts, mixer, funnel, tray, box, tablet pressing tools and other products for the production of drugs, diagnosis, cosmetics and food. It is convenient for repeated verification and cleaning record preservation. The same batch of cleaning equipment has a good uniformity, there will be no manual cleaning of some utensils do not meet the requirements of the experimental failure phenomenon, saving the time of the experimenter.
Technical performance and characteristics: 1. Instrument structure: shell material, 304 stainless steel, inner cavity material, 316L stainless steel; cleaning volume: 1050 L 2. Double circulation pump structure design, circulation capacity: 800L / min / pump, total circulation capacity: 1600L / min; circulation pump adopts soft start control to prevent vessels from being impacted at the moment of pump start-up 3. Water source type: tap water, purified water, condensate water, injection water The water flow meter has built-in pipeline to calculate the water inflow in real time The inner water tank is equipped with low and high liquid level alarm devices to ensure the safety of cleaning water 4. Safety protection system: door closing anti pinch hand, both hands closing, water heating over temperature protection, hot air heating over temperature protection, water pump over temperature protection, fan over temperature protection, water leakage real-time monitoring protection, leakage protection 5. The running status indicator is placed on the top of the machine, and the running machine status is displayed in real time through green, yellow and red 6. The cleaning conforms to en iso15883 standard, and the manufacturer has passed ISO9001, ISO14001 and iso45001 certification 7. Cleaning verification: the company has passed the ISO9001 certification, and ensures the development and construction of the system with high quality awareness. According to the cGMP and gamp guidelines, the controlled process conforms to FDA directives, IQ / OQ and fat / Sat. as part of factory acceptance (fat), according to urs / Fs, the cleaning equipment is checked to see if it meets the requirements according to the standard language bottle agreement. Trained bottle professionals can set up, connect, and put into service cleaning systems, calibrate, and perform installation and operational qualification / functional qualification (IQ / OQ) and support in performance qualification (PQ). It is necessary to provide printer, print cleaning data, provide USB interface, automatically store cleaning data, export cleaning data from USB flash disk, and audit and track operation records 8. CE / FDA 21 CFR Part 11: Electronic Records 9. Drying system: double compression fan drying system, hot air circulation capacity is not less than 145m3 / h / fan, fan power: 700W, dry air directly to the interior of the container through the injection cleaning rack, the temperature can be adjusted (room temperature - 120 ℃), drying time (0-300 minutes), with double spray heat exchange system, steam condensation
Introduction: Our pharmaceutical industry and life science industry cleaning system is used to clean key components, such as fermentation tank, atmospheric sphere bottle, large glass products, filling and packaging machine parts, mixer, funnel, tray, box, tablet pressing tools and other products for the production of drugs, diagnosis, cosmetics and food. It is convenient for repeated verification and cleaning record preservation. The same batch of cleaning equipment has a good uniformity, there will be no manual cleaning of some utensils do not meet the requirements of the experimental failure phenomenon, saving the time of the experimenter.
