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Double HEPA-ness for double protection with the new Coway Double HEPA Filter

New filter is proven to reduce up to 99.999% of COVID-19 Omicron variant

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Air pollution is everywhere

and it can be worse indoors than outdoors.

 

It is especially crucial now with the surge of COVID-19 virus which increases the risk of harmful pollutants in our indoor air.

While most airborne particles and various viruses are invisible to the human eye, you will be protected with Coway’s state-of-the-art Double HEPA Filter air purifying technology.

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Double HEPA Filter

Reduces ultrafine particles like viruses and bacteria

Double HEPA Filter technology offers double protection with its antibacterial coating of Copper(Cu) and Zinc Pyrithione. The Double HEPA Filter is certified to reduce up to 99.999% of COVID-19 virus including Omicron variant, Influenza A H1N1, bacteria, black mold and more.

To inhibit the spread of these harmful pollutants, the filter’s antibacterial performance inactivates cell membranes and protein structures of viruses. Within 24 hours, these pollutants are inactivated and inhibited from spreading.

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Double HEPA Filter Technology

Stay Protected With Lombok III And Storm
Fit In With Coway Double Hepa Filter

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LOMBOK III

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STORM

Disclaimer:

 

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.