Mask Bacterial Filtration Efficiency Tester

Medicinska masker bakteriella filtreringseffektivitetstester

The Mask Bacterial Filtration Efficiency Tester is used to measure the Bacterial Filtration Efficiency (BFE) of medical and surgical masks to determine their protective performance against airborne bacterial contamination. The tester is compatible with EN14683, ASTM F2100, ASTM F2101, YY 0469, and YY0969.

A bacterial suspension is pumped into a nebulizer, and the aerosol is propelled into an aerosol chamber. It is then delivered to two Anderson sieve samplers—one with a test sample and the other without—to compare the results.

The two Anderson sieve samplers enable simultaneous results with and without the test sample, minimizing bias. The machine features a built-in, clear, three-stage cleaning system (disinfectant solution, purified water, airflow) to ensure safety after testing.

Instrument characteristics

1. Professionell negativtryck biologisk säkerhet skåp teknik för att säkerställa säkerheten för operatörer och miljön.

2. Högt negativt tryck arbetskabin, tvåstegs högeffektivt filter, 100% säker urladdning.

3. Anta tvåvägs sex-nivå Anderson exakt provtagning.

4. Inbyggd peristaltisk pump med justerbar flödeshastighet.

5. Speciell mikrobiell aerosolgenerator, flödeshastigheten av bakteriell vätskespray är justerbar och atomiseringseffekten är bra.

6. industriell kvalitet stor färg pekskärm kontroll, operationen är enklare.

7. Kontrollsystemet antar PLC + LabView kontroll, hög intensitet färg pekskärm 10 tum, USB gränssnitt, stöder U disk dataöverföring;

8. Säkerhetsskåpet har inbyggd LED-belysning för enkel observation.

9. Inbyggd ultraviolett desinfektionslampa för att förbättra skyddseffekten.

10. Den främre brytaren typ förseglad glasdörr är bekväm för drift och observation.

11. Med operativprogramvara kan den styras och bearbetas av dator.

12. Sömlöst ansluta laboratorieinformationshanteringssystemet.

Mask Filtration Effectiveness Testing

① According to the medical surgical mask standard YY0469-2011. connect the two sampling ports of the Henderson pipe of the BFE system detector to the Anderson six-stage sampler.

② Load a 90mm diameter sampling plate into the Anderson six-stage sampler. Control the sampler's gas flow rate at 28.3L/min, the peristaltic pump flow rate at 0.180mL/min, the liquid supply time at 1min, the sampling time at 2min, and the system cleaning time at 1min. Perform a positive quality control test before testing.

③ After the sample test is complete, perform another positive quality control test. Then, collect an air sample from the aerosol chamber for 2min as a negative quality control. During this process, do not feed the bacterial suspension into the nebulizer.

④ Place the agar plate upside down in a (37±2)°C incubator and incubate for (48±2)h.

Then count the colony forming units (positive wells) of the bacterial particle aerosol and convert them to the number of possible impacting particles using a positive well conversion table. The formula for calculating the bacterial filtration efficiency of a mask is: BFE = (C-T)/C × 100% (where C is the average value of the positive quality control; T is the sum of the sample counts). The "Technical Requirements for Medical Surgical Masks" (YY 0469-2011) stipulates that the bacterial filtration efficiency should be greater than 95%.

Medical surgical masks can effectively prevent the spread of pathogens and protect healthy people. BFE is expressed as the percentage of aerosols filtered by the medical surgical mask filter material at a specified flow rate and is an important parameter for evaluating the performance of medical surgical masks [4.5]. The BFE system generates bioaerosols in an artificially controlled environment and evaluates the protective performance and safety of medical surgical masks by calculating the microbial aerosol filtration efficiency. The system program has three modes: purification, maintenance, and testing. This program not only ensures the accuracy of experimental results but also ensures the safety of experimental personnel, experimental samples, and the experimental environment.

Regular Maintenance

If water droplets are present in the water separator and aerator, loosen the knob at the bottom of the water separator and air filter to drain the water. After draining, re-tighten the knob. The HEPA filter included with the detector is a consumable item and should normally be replaced once a year.

Daily Maintenance: This detector should be used in a well-ventilated, dry, dust-free environment free from strong electromagnetic interference. The power cord may become loose or disconnected after long-term use. Inspect the power cord before each use to ensure it is free of damage, cracks, or disconnections.

Clean the instrument with a soft cloth and a neutral detergent. Before cleaning, disconnect the power cord. Do not use volatile substances such as thinners and benzene to clean the instrument, as these may change the color of the instrument housing, erase the markings on the housing, or blur the touchscreen display.