Laboratory Equipment>Dehumidifier
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23. Botai Purification Workbench S · SW-CJ-2F Type 1360 × seven hundred × 460 type
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25. Botai Purification Workbench S · SW-CJ-1F Type 870 × seven hundred × 520mm
26. Botai Purification Workbench S · SW-CJ-1CU Type 1680 × four hundred and eighty × 600mm
27. Botai Purification Workbench S · SW-CJ-1C Type 1680 × four hundred and eighty × 600mm
28. Botai Purification Workbench S · SW-CJ-1BU Type 820 × four hundred and eighty × 600mm
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BIOBASE Boke Dispensing Cabinet PYG1200-C
Product Introduction
The medicine dispensing cabinet (also known as constant temperature medicine dispensing cabinet/chemotherapy medicine dispensing cabinet, etc.) adopts the technology of efficient air purification, drug test lamp, and automatic heating medicine solution, which can provide a local high cleanliness air environment for medicine dispensing. The negative pressure type can protect the operator and the room Internal environment.
It is suitable for centralized or decentralized use in various departments of hospitals, and is suitable for use in ICUs, preparation rooms, outpatient clinics, and emergency departments. (It is commonly used in the oncology department of hospitals.)
Product advantages
Pre heating and optical clarity testing can be performed on the prepared medicinal solution.
technical parameter
External dimensions: 1200mm× 695mm× 2200mm;
Operating area size: 1120mm× 540mm× 600mm
Power requirement AC: 220V 50Hz;
Dust (for≥ 0.5um):≤ 3.5 capsules/liter;
Purification efficiency (for≥ 0.5um dust particles): 99.99%;
Average vertical descending wind speed: 0.3 m/s;
Light intensity: The average illuminance should be≥ 300lux;
Lighting 21W× 1;
Applicable scope
This dispensing cabinet is specially designed and developed for the dispensing operation before infusion treatment in hospitals. The dispensing cabinet adopts technologies such as efficient air purification, drug testing lights, and self-control heating of the medication solution, which can create a local high cleanliness dispensing operation air environment and can pre heat and light check the clarity of the dispensed medication solution. It can be used centrally or dispersedly in various departments of the hospital, and is suitable for use in ICUs, preparation rooms, outpatient clinics, and emergency departments.
work environment
Only applicable indoors;
Environmental temperature: 15 ℃~35 ℃;
Relative humidity:≤ 75%;
Atmospheric pressure range: 70kPa~106kPa;
Power supply: AC 220V, 50Hz, with good grounding;
Power: 800W.
Product Features
The dispensing cabinet is equipped with a negative pressure air duct, which forms an air curtain and double layer isolation between the working area and the external environment. At the same time, the working area is surrounded by positive pressure airflow, ensuring that the drugs are not contaminated by indoor air;
The box is made of 1.2mm thick cold-rolled steel plate, which enhances the structural strength and makes the entire device more stable;
The workbench in the work area is made of stainless steel material, which is beautiful and corrosion-resistant;
The control panel adopts touch switches, making the machine appearance beautiful and easy to operate;
Digital temperature and pressure difference display.
Operating instructions
1. Connect a 220V, 50HZ AC power supply;
If the air supply and exhaust filters of the equipment fail to meet the specified requirements, the equipment will sound and light an alarm, prompting the user to immediately replace the filter to protect their safety;
3. Press the power button, and the pressure difference display defaults to the supply air pressure difference, with a value of zero;
After pressing the power button, other function keys can only be used: lighting, heating and insulation, fan, air volume adjustment, and display content switching.
5. Before dispensing, turn on the dispensing cabinet fan to purify the air for 30 minutes. After purifying the dispensing room, proceed with the dispensing operation;
6. Clarity Light Test Method: When performing a light test on the clarity of the drug solution, invert the bottle containing the drug solution under a light without illuminating the bottle. Use a white lining to observe the dark impurities in the drug solution, and then illuminate the bottle with a light. Use a matte black lining to observe the light colored impurities in the drug solution. If any abnormal phenomena such as turbidity, sedimentation, crystallization, or discoloration are found during the dispensing process, the operation should be stopped immediately, and the cause should be identified and resolved before continuing;
7. The temperature displayed on the control panel is the gas temperature at the measuring point of the temperature sensor, not the temperature of the liquid medicine in the bottle. Generally, the liquid medicine in the bottle can reach 30~37 ℃ when the control panel displays 30~35 ℃ after it is put into the heating incubator to be heated for 2~4 hours. Therefore, the liquid medicine to be prepared should be put into the heating incubator Negage 2~4 hours before the dispensing operation.
8. Please confirm whether the patient needs to use heated medication, or whether the patient's condition is suitable for using heated medication.
Please confirm if the drug can be heated without causing any quality changes.
matters needing attention
Before connecting to the AC power supply, ensure that the voltage of the power supply is consistent with the input voltage of the dispensing cabinet and stable, and ensure that the rated load of the power socket is not less than this requirement; This dispensing cabinet uses a grounding plug, which has a third pin and can only be used with a grounded power socket. This is a safety device. If the plug cannot be inserted into the socket, an electrician should be asked to install a grounded power socket;
2. During the use of the equipment, do not place soft or delicate items (such as soft tissue) on the countertop to prevent them from being sucked into the negative pressure air duct and fan by the suction port, which may affect the operation of the equipment;
3. Avoid vibration: Try to avoid the use of vibrating instruments (such as centrifuges, vortex oscillators, etc.) inside the cabinet, as vibration can shake off particulate matter accumulated on the filter membrane, resulting in a decrease in the cleanliness of the operating room. At the same time, if the balance on the front operating surface fails, it will also cause contamination of the dispensing cabinet to the operator;
4. Prohibition of open flames: Open flames are prohibited in the dispensing cabinet! During the use of open flames, it can cause disordered airflow in the dispensing cabinet and damage the filter. During the experiment, high-temperature disinfection and sterilization are required, and it is strongly recommended to use an infrared sterilizer;
5. High efficiency filters have a lifespan. With the extension of their lifespan, the accumulation of dust and bacteria in the filter can lead to an increase in pressure loss of the high efficiency filter. When the pressure increases to an alarm sound, it is necessary to contact our company's service department in a timely manner to replace the high efficiency filter, otherwise it will affect the safety performance of the equipment. The replaced filter should be disposed of as medical waste.
6. The fan and its lower steel plate are static pressure box covers, and the rear side door is a negative pressure air duct baffle. These air ducts have undergone strict sealing treatment before leaving the factory, and their sealing properties must be maintained. The operator must not loosen or remove the screws of these components. If there is a special need, it must be handled by our company's service personnel;
7. The grille near the front of the countertop is used for air intake. When operating the dispensing cabinet, do not block the grille as it will affect the airflow of the dispensing cabinet. Suggest using a hand rest to solve this problem and reduce wrist fatigue for operators;
8. The total weight of all items hanging on the hook should not exceed 5kg;
9. The storage period of the equipment is one year. If it exceeds the storage period, it must be unpacked and inspected by our company's technical personnel once, and can only be used after passing the inspection.
Solemnly declare that our company will not be responsible for the risks caused by non compliant operations!
