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1. Advanced 6-Step Filtration reduce up to 99.999% Ultrafine Dust and 99.9% Airborne viruses, bacteria, black mold

1. Negative ion generation test, Test Institute: Korean Analysis Test Researcher (KATR), Test Environment: Sunny, 21.4℃, 31% RH (Relative Humidity), Measuring Range: 0-2,000,000 ea/cc (if 2,000,000 ea/cc measured, marked as over 2,000,000 ea/cc), Test Methods: Setting device’s mode to TURBO, PLASMA and ION. Aging for 10 minutes and operate the device for 1 hour. After that, install the air sampler inlet at a distance of 10 cm from the machine outlet and operate for 60 minutes. Test Result: Negative ion generation is over 2,000,000 ea/cc. The indicated value is indicated within the error range of the test result of the evaluation institution, and since the measured value is calculated in a closed experimental environment, it may vary in the use environment.

2. Purification ability test, test Institute: DT & C Co., Ltd., Test Method: Tested according Korean Air Cleaning Association to SPS-KACA 002-0132:2018 Indoor Air Cleaners, Test Condition: Temperature 23±5 ℃, Humidity 55±15%, Test Chamber: 29.6m3. Test Result: CADR OF 384m3/h OR 6.4m3/min. The indicated value is indicated within the error range of the test result of the evaluation institution, and since the measured value is calculated in a closed experimental environment, it may vary in the use environment.

3. Ultrafine particle (0.01 ㎛) removal test, test content: 0.01 ㎛ diameter particle removal efficiency,Test Content: 0.01 ㎛ diameter particle removal efficiency (model tested: AP-1520C), Test Specification: Tested accordin+C5:I6g to Korean Air Cleaning Association SPS-KACA 002-132:2018, Indoor air purifier, Test Condition: Temperature 23.0±1.0 ℃, Humidity 50.0±1.5%, Test Chamber: 30m3, Test Method: Measure the removal rate of 0.01 ㎛ diameter fine particles within 40 mins by operating the air purifier in the test chamber at the rated air volume. Test Result: Ultrafine dust removed by 99.999% and germs removed by 99.9%The indicated value is indicated within the error range of the test result of the evaluation institution, and since the measured value is calculated in a closed experimental environment, it may vary in the use environment.

4. Virus Removal Test, Test Institute: Korea Conformity Laboratories (KCL), Test Standard: According to ISO 16000-36:2018, Test Condition: Temperature 23±0.2, Humidity 50.5±3.0 %, Test Chamber: 30 ㎥, Test strain: MS2 ATCC 15597-B1, Phi-X174 ATCC 13706-B1, Test Methods: Evaluate the reduction rate compared to the initial virus concentration by operating the air purifier in the test chamber at the rated air volume for 1 hour. Test Result: Virus removed by 99.9%. The indicated value is indicated within the error range of the test result of the evaluation institution, and since the measured value is calculated in a closed experimental environment, it may vary in the use environment.

5. Airborne bacteria removal test, Test Institute: Korea Conformity Laboratories (KCL), Test Standard: Tested according to ISO 16000-36:2018, Test Condition: Temperature 23±0.2 ℃, Humidity 50.5±3.0%, Test Chamber: 30m3, Test Strain: Escherichia coli ATCC 25922 (E. coli), Staphylococcus aureus ATCC6538, Klebsiella pneumonia ATCC4352, Pseudomonas aeruginosa ATCC15442, MRSA (Methacillin-resistant Staphylococcus aureus) ATCC33591, Test Methods: Evaluate the reduction rate compared to the initial concentration of bacteria by operating the air purifier in the test chamber at the rated air volume for 1 hour, Test Result: Airborne Bacteria removed by 99.9%, The indicated value is indicated within the error range of the test result of the evaluation institution, and since the measured value is calculated in a closed experimental environment, it may vary in the use environment.

6. Airborne Black Mold Removal, Test Institute: Korea Conformity Laboratories (KCL), Test Standard: According to ISO 16000-36:2018, Test Condition: Temperature 23±0.2, Humidity 50.5±3.0 %, Test Chamber: 30m3, Test strain: Aspergillus brasiliensis ATCC 9642, Test Methods: Run the air purifier in the test chamber at the rated air volume for 1 hour to evaluate the reduction rate compared to the initial bacterial concentration. Test Result: Airborne Black Mold removed by 99.9% The indicated value is indicated within the error range of the test result of the evaluation institution, and since the measured value is calculated in a closed experimental environment, it may vary in the use environment.

7. Mold Reduction (Mixed 5 Strains), Test Institute: Korea Conformity Laboratories (KCL), Test Standard: Accoridng to ISO/IEC 17025 and KOLAS. Test Method: ASTM G 21-15, Test Condition: Temperature 29±0.2, Humidity 92.8±2.0 %, Test strain: Aspergillus brasiliensis ATCC 9642, Penicillium Funiculosum ATCC 11797, Chaetomium Globosum ATCC 6205, Trichoderma Virens ATCC 9645, Aureobasidium Pullulans ATCC 15233. Test Result: Mold removed by 99.9% .The indicated value is indicated within the error range of the test result of the evaluation institution, and since the measured value is calculated in a closed experimental environment, it may vary in the use environment.

 

2. Double HEPA with advanced filter materials reduce up to 99.999% of COVID-19 virus, Omnicron variant, Influenza A H1N1 with its antibacterial performance.

1. SARS CoV-2 Omicron Variant Removal, Test Institute: College of Veterinary Medicine Jeonbuk National University, Test Subject: Double HEPA filter, Test Method: Measurement of virus constraint effect of Double HEPA filter. Analysis Of Plaque: Test strain applied on the material of the Double HEPA filter measured after 4hours and 24 hours., Strain Tested: SARS Cov-2 Omicron Variant. Test Result: 99.999% reduction after a 4-hour reaction. The indicated value is indicated within the error range of the test result of the evaluation institution, and since the measured value is calculated in a closed experimental environment, it may vary in the use environment.

2. Human Corona Virus (HCoV-OC43) Inactivation, Test Institute: BioPS Co., Ltd., Test Method: Evaluation of coronavirus inactivation efifacy mesured after 12 hours and 24 hours. Strain Tested: Human coronavisrus OC43 (HCoV-OC43) as the model Virus of SARS-Cov-2. Test Result: Above 99.999% virus inactivation. The indicated value is indicated within the error range of the test result of the evaluation institution, and since the measured value is calculated in a closed experimental environment, it may vary in the use environment.

3. Influenza A Virus H1N1, Test Institute: BioPS Co., Ltd., Test Method: Evaluation of influenza virus inactivation effifacy mesured after 12 hours and 24 hours. Strain Tested: Influenza A Virus Subtype H1N1. Test Result: 99.95% inactivation. The indicated value is indicated within the error range of the test result of the evaluation institution, and since the measured value is calculated in a closed experimental environment, it may vary in the use environment.

4. Antibacterial Performance, Test Institute: Korean Analysis Test Researcher (KATR), Test Strain: Staphylococcus aureus ATCC 6538, Escherichia coli ATCC 8739, Klebsiella pneumoniae ATCC 4352. Test Result: 99.9% reduction rate. The indicated value is indicated within the error range of the test result of the evaluation institution, and since the measured value is calculated in a closed experimental environment, it may vary in the use environment.

5. Antibacterial Performance, Test Institute: FITI Testing And Research Institute, Test Strain: Escherichia coli ATCC 25922, Test Result: 99.9% reduction rate. The indicated value is indicated within the error range of the test result of the evaluation institution, and since the measured value is calculated in a closed experimental environment, it may vary in the use environment.