Coway

Coway

Coway

Coway

Coway

Coway

¹ Van Coway luchtreinigers is bewezen dat ze de lucht zuiveren van stof, pollen, huidschilfers, virussen en bacteriën volgens tests die zijn uitgevoerd door KCL (Korea Conformity Laboratories). Om de verwijdering van deeltjes met een grootte tot 0,01 µm te meten, werden de luchtreinigers getest volgens de normen van de Korea Air Cleaning Association (SPS-KACA 002-132:2018 Modified) in een ruimte van 30 m³. De test vond plaats bij maximale ventilatorsnelheid, onder normale kamertemperatuur- en vochtigheidsomstandigheden. De resultaten kunnen variëren in de werkelijke leefomgeving van de gebruiker.. ² 99,9% van de virussen, bacteriën, schimmels en pollen werden aantoonbaar uit de lucht gereinigd door de Coway luchtreiniger met toegepast GreenHEPA filter, zoals getest door de Japan Food Research Laboratories (JFRL) volgens de JEM 1467 norm.. Getest met de AIRMEGA AP-1516D, AIRMEGA AP-1220B, AIRMEGA MIGHTY luchtreinigers, alsmede de AIRMEGA 150, AIRMEGA 250, AIRMEGA 300S. AIRMEGA 400S zal getest worden in 1H, 2022.. Alle door JFRL geteste producten hebben de bovenstaande resultaten behaald, beneden de vooraf vastgestelde tijd.. Virus: getest met Escherichia Coli Phage ΦX174 NBRC 103405, 60 minuten. Bacteriën: getest met Staphylococcus epidermidis NBRC 12993, 60 minuten. Schimmels: getest met Penicillium citrinum NBRC 6352, 60 minuten. Pollen: getest met Cedar Pollen extract, 30 minuten.. Getest met het Influenza A virus (H1N1) en Staphylococcus aureus op de GreenHEPA filter van Coway, door Japan Food Research Laboratories (JFRL). Na 24 uur testen bij kamertemperatuur werd geen groei van het materiaal waargenomen.. Beide testen waren gedaan op kleine proefstukken, die van het GreenHEPA-filter gesneden waren. Daarom geldt deze disclaimer voor alle Coway-producten die dit  GreenHEPA-filter gebruiken.. Virus: getest met Influenza A virus (H1N1), 3 cm x 3 cm op geautoclaveerd stuk. Bacteriën: getest met Staphylococcus aureus, geënt op 50 mm x 50 mm proefstuk.. ³ Getest met Humaan Coronavirus (HCoV-OC43) op de GreenHEPA technologie filter van Coway door BioPS Co., Ltd, een research organisatie dat zich specialiseert in virale opruiming onderzoeken in Zuid Korea. De testmethode was een filter media test om de effectiviteit van de neutralisatie te testen. Na het gedurende 2 uur lang behouden van het testmateriaal in kamertemperatuur, was er boven 99,999% verwijderingspercentage van het virus, nadat het virus contact had gemaakt met de filter media, waarmee is bewezen dat het virus geneutraliseerd of geïnactiveerd was. Hetzelfde resultaat bleek na 12 uur en 24 uur. Deze specifieke test is gedaan met het Humaan Coronavirus HCoV-OC43 als test-virus (niet Covid-19 SARS-CoV-2), omdat OC-43 een van de 7 types Coronavirussen is waar een mens mee geïnfecteerd kan raken.. NB: Van luchtreinigers is bekend dat ze effectief zijn in het voorkomen van Covid-19. Echter zou dit nooit gezien moeten worden als de primaire manier om infectie tegen te gaan. Handen goed schoonmaken, contact mijden en niet in kleine, slecht-geventileerde publieke ruimtes bevinden zijn allemaal belangrijk om infectie tegen te gaan. Coway staat achter elke patiënt en al medisch personeel wereldwijd die onvermoeibaar werken om dit virus en andere virussen tegen te gaan.. * De CADR (Clean Air Delivery Rate) van deeltjes wordt getest volgens GB / T18801-2015 door een gecertificeerd, onafhankelijk laboratorium.. - De meetspecificaties zijn vastgelegd in GB/T 18801-2015, waarbij twee vervalsnelheden van de deeltjesconcentratie moeten worden bepaald binnen een testkamer met een gedefinieerd volume (Vkamer): een natuurlijk verval met een inactief luchtfilter (knat) en een verval tijdens een meting in een testkamer van 30 m3. Deze testkamer is leeg - met uitzondering van het luchtfilter dat op een tafel is geplaatst. Twee ventilatoren mengen en circuleren de lucht. Bovendien bevinden zich in deze kamer ook een paar meetapparaten (voornamelijk slangen).. De kamer wordt op een temperatuur van 25 (± 2 ° C) en een relatieve vochtigheid van 50 (± 10 %) gehouden.. Als test-aërosol wordt sigarettenrook gebruikt. Het aantal deeltjes > 0,3 µm wordt gemeten met een optische aërosol-spectrometer die gebruik maakt van het interne luchtfilter (kAC).. De vervalsnelheden "k" worden bepaald aan de hand van het gemeten tijdsverval van de deeltjesconcentratie C (t), uitgaande van de beginconcentratie C = 0.. *  De kamergrootte wordt berekend volgens de norm NRCC-54013. Hier wordt de CADR getest volgens GB / T18801-2015.. NRCC: Methode voor testen van luchtreinigers. Formula for room size: Room size = 0,26*CADR. NB: Testresultaten kunnen variëren, afhankelijk van de werkelijke gebruiksomgeving van de klant.

3-traps filtratie, Dynamisch bereik van 360 graden, Auto-oscillatie tot 80°, Multi-verticaal kantelen tot 90°, Afstandsbediening, Energiebesparend in Auto-mode

¹ Coway air purifiers has been proven to trap dust, pollen, dander, viruses, and bacteria in the air based on KCL (Korea Conformity Laboratories) testing. They have been tested in a 30㎥-size chamber according to the Korea Air Cleaning Association standard (SPS-KACA 002-132:2018 Modified) to measure the 0.01㎛ size of particle removal rate. It was tested on maximum fan speed in normal room temperature and humidity conditions. The performance may vary in the actual living environment of customers.. ² 99.9% of viruses, bacteria, fungi, and pollen were verified to be removed from the air by Coway air purifiers with GreenHEPA™ technology applied filters based on the Japan Food Research Laboratories (JFRL) testing according to JEM 1467 standard. Tested with AIRMEGA AP-1516D, AIRMEGA AP-1220B, AIRMEGA MIGHTY air purifiers and additionally AIRMEGA 150, AIRMEGA 250, AIRMEGA 300S, AIRMEGA 400S will acquire the test report in 1H, 2022.. All tested by JFRL and received above result within below time.. Virus: Tested with Escherichia coli phage ΦX174 NBRC 103405, 60 minutes. Bacteria: Tested with Staphylococcus epidermidis NBRC 12993, 60 minutes. Fungi/Mold: Tested with Penicillium citrinum NBRC 6352, 60 minutes. Pollen: Tested with Cedar Pollen extract, 30 minutes. Tested with Influenza A virus (H1N1) and Staphylococcus aureus on Coway’s Green HEPA filter media by Japan Food Research Laboratories (JFRL) and no growth was found on the material after 24 hours kept in room temperature.. Both tests were performed on small test pieces cut from the Green HEPA filter media, so this disclaimer can be used for any Coway products that use this filter.. Virus: Tested with Influenza A virus (H1N1), 3cm x 3cm autoclaved piece. Bacteria: Staphylococcus aureus, inoculated on 50mm x 50mm test piece.. ³ Tested with Human Coronavirus (HCoV-OC43) on Coway GreenHEPA™ technology applied filter media by BioPS Co., Ltd, a research organization specializing in viral clearance studies in South Korea. The test method was a filter media coupon test to observe the neutralization effectiveness. After 2 hours kept in room temperature, there was above 99.999% removal rate of the virus after the virus made contact with the filter media resulting in neutralization or inactivation of the virus is valid. Same result shows after 12 hours and 24 hours. This specific test was conducted with Human Coronavirus (HCoV-OC43) as the experimental model virus (Not Covid-19 (SARS-CoV-2)) because OC-43 is one of the seven types of Coronaviruses that can be infected to human.. Note: Air purifiers are known to be effective in preventing the Covid-19. However, it should never be regarded as the primary method of virus infection. Cleaning hands, trying to avoid contact and avoiding being in closed space in public is necessary to minimize the possibility of being affected by possible virus infection. Coway supports every patient and medical staff around the world who work tirelessly to prevent and cure the spread of hazardous viruses.. * CADR (Clean Air Delivery Rate) of particulate matter is tested according to GB/T18801-2015 by a certified third-party lab.. Measurement specifications are defined in GB/T 18801-2015, according to which two particle concentration decay rates have to be determined within a test chamber with a defined volume (Vchamber): a natural decay rate with inactive air cleaner (knat) and a decay rate detected under the measurements are carried out in a 30 ㎥chamber, which is empty except for the air cleaner placed on a table, two fans to mix and recirculate the air and some measurement periphery (mainly tubing). The chamber is kept at a temperature of 25 ± 2°C and a relative humidity of 50 ± 10%. Cigarette smoke is used as test aerosol and the number concentration of particles > 0.3 µm is measured using an optical aerosol spectrometer usage of the indoor air cleaner (kAC). The decay rates k is determined from the measured temporal decay of the particle concentration C(t), starting from the initial concentration C0:. * Room size is calculated according to NRCC-54013 standard using CADR tested according to GB/T18801-2015.. NRCC: Method for Testing Air Cleaners. Formula for room size: Room size = 0.26*CADR. Note: The performance results may vary depending on the actual use environment of customers.

¹ Coway air purifiers has been proven to trap dust, pollen, dander, viruses, and bacteria in the air based on KCL (Korea Conformity Laboratories) testing. They have been tested in a 30㎥-size chamber according to the Korea Air Cleaning Association standard (SPS-KACA 002-132:2018 Modified) to measure the 0.01㎛ size of particle removal rate. It was tested on maximum fan speed in normal room temperature and humidity conditions. The performance may vary in the actual living environment of customers.. ² 99.9% of viruses, bacteria, fungi, and pollen were verified to be removed from the air by Coway air purifiers with GreenHEPA™ technology applied filters based on the Japan Food Research Laboratories (JFRL) testing according to JEM 1467 standard. Tested with AIRMEGA AP-1516D, AIRMEGA AP-1220B, AIRMEGA MIGHTY air purifiers and additionally AIRMEGA 150, AIRMEGA 250, AIRMEGA 300S, AIRMEGA 400S will acquire the test report in 1H, 2022.. All tested by JFRL and received above result within below time.. Virus: Tested with Escherichia coli phage ΦX174 NBRC 103405, 60 minutes. Bacteria: Tested with Staphylococcus epidermidis NBRC 12993, 60 minutes. Fungi/Mold: Tested with Penicillium citrinum NBRC 6352, 60 minutes. Pollen: Tested with Cedar Pollen extract, 30 minutes. Tested with Influenza A virus (H1N1) and Staphylococcus aureus on Coway’s Green HEPA filter media by Japan Food Research Laboratories (JFRL) and no growth was found on the material after 24 hours kept in room temperature.. Both tests were performed on small test pieces cut from the Green HEPA filter media, so this disclaimer can be used for any Coway products that use this filter.. Virus: Tested with Influenza A virus (H1N1), 3cm x 3cm autoclaved piece. Bacteria: Staphylococcus aureus, inoculated on 50mm x 50mm test piece.. ³ Tested with Human Coronavirus (HCoV-OC43) on Coway GreenHEPA™ technology applied filter media by BioPS Co., Ltd, a research organization specializing in viral clearance studies in South Korea. The test method was a filter media coupon test to observe the neutralization effectiveness. After 2 hours kept in room temperature, there was above 99.999% removal rate of the virus after the virus made contact with the filter media resulting in neutralization or inactivation of the virus is valid. Same result shows after 12 hours and 24 hours. This specific test was conducted with Human Coronavirus (HCoV-OC43) as the experimental model virus (Not Covid-19 (SARS-CoV-2)) because OC-43 is one of the seven types of Coronaviruses that can be infected to human.. Note: Air purifiers are known to be effective in preventing the Covid-19. However, it should never be regarded as the primary method of virus infection. Cleaning hands, trying to avoid contact and avoiding being in closed space in public is necessary to minimize the possibility of being affected by possible virus infection. Coway supports every patient and medical staff around the world who work tirelessly to prevent and cure the spread of hazardous viruses.. * CADR (Clean Air Delivery Rate) of particulate matter is tested according to GB/T18801-2015 by a certified third-party lab.. Measurement specifications are defined in GB/T 18801-2015, according to which two particle concentration decay rates have to be determined within a test chamber with a defined volume (Vchamber): a natural decay rate with inactive air cleaner (knat) and a decay rate detected under the measurements are carried out in a 30 ㎥chamber, which is empty except for the air cleaner placed on a table, two fans to mix and recirculate the air and some measurement periphery (mainly tubing). The chamber is kept at a temperature of 25 ± 2°C and a relative humidity of 50 ± 10%. Cigarette smoke is used as test aerosol and the number concentration of particles > 0.3 µm is measured using an optical aerosol spectrometer usage of the indoor air cleaner (kAC). The decay rates k is determined from the measured temporal decay of the particle concentration C(t), starting from the initial concentration C0:. * Room size is calculated according to NRCC-54013 standard using CADR tested according to GB/T18801-2015.. NRCC: Method for Testing Air Cleaners. Formula for room size: Room size = 0.26*CADR. Note: The performance results may vary depending on the actual use environment of customers.

¹ Coway air purifiers has been proven to trap dust, pollen, dander, viruses, and bacteria in the air based on KCL (Korea Conformity Laboratories) testing. They have been tested in a 30㎥-size chamber according to the Korea Air Cleaning Association standard (SPS-KACA 002-132:2018 Modified) to measure the 0.01㎛ size of particle removal rate. It was tested on maximum fan speed in normal room temperature and humidity conditions. The performance may vary in the actual living environment of customers.. ² 99.9% of viruses, bacteria, fungi, and pollen were verified to be removed from the air by Coway air purifiers with GreenHEPA™ technology applied filters based on the Japan Food Research Laboratories (JFRL) testing according to JEM 1467 standard. Tested with AIRMEGA AP-1516D, AIRMEGA AP-1220B, AIRMEGA MIGHTY air purifiers and additionally AIRMEGA 150, AIRMEGA 250, AIRMEGA 300S, AIRMEGA 400S will acquire the test report in 1H, 2022.. All tested by JFRL and received above result within below time.. Virus: Tested with Escherichia coli phage ΦX174 NBRC 103405, 60 minutes. Bacteria: Tested with Staphylococcus epidermidis NBRC 12993, 60 minutes. Fungi/Mold: Tested with Penicillium citrinum NBRC 6352, 60 minutes. Pollen: Tested with Cedar Pollen extract, 30 minutes. Tested with Influenza A virus (H1N1) and Staphylococcus aureus on Coway’s Green HEPA filter media by Japan Food Research Laboratories (JFRL) and no growth was found on the material after 24 hours kept in room temperature.. Both tests were performed on small test pieces cut from the Green HEPA filter media, so this disclaimer can be used for any Coway products that use this filter.. Virus: Tested with Influenza A virus (H1N1), 3cm x 3cm autoclaved piece. Bacteria: Staphylococcus aureus, inoculated on 50mm x 50mm test piece.. ³ Tested with Human Coronavirus (HCoV-OC43) on Coway GreenHEPA™ technology applied filter media by BioPS Co., Ltd, a research organization specializing in viral clearance studies in South Korea. The test method was a filter media coupon test to observe the neutralization effectiveness. After 2 hours kept in room temperature, there was above 99.999% removal rate of the virus after the virus made contact with the filter media resulting in neutralization or inactivation of the virus is valid. Same result shows after 12 hours and 24 hours. This specific test was conducted with Human Coronavirus (HCoV-OC43) as the experimental model virus (Not Covid-19 (SARS-CoV-2)) because OC-43 is one of the seven types of Coronaviruses that can be infected to human.. Note: Air purifiers are known to be effective in preventing the Covid-19. However, it should never be regarded as the primary method of virus infection. Cleaning hands, trying to avoid contact and avoiding being in closed space in public is necessary to minimize the possibility of being affected by possible virus infection. Coway supports every patient and medical staff around the world who work tirelessly to prevent and cure the spread of hazardous viruses.. * CADR (Clean Air Delivery Rate) of particulate matter is tested according to GB/T18801-2015 by a certified third-party lab.. Measurement specifications are defined in GB/T 18801-2015, according to which two particle concentration decay rates have to be determined within a test chamber with a defined volume (Vchamber): a natural decay rate with inactive air cleaner (knat) and a decay rate detected under the measurements are carried out in a 30 ㎥chamber, which is empty except for the air cleaner placed on a table, two fans to mix and recirculate the air and some measurement periphery (mainly tubing). The chamber is kept at a temperature of 25 ± 2°C and a relative humidity of 50 ± 10%. Cigarette smoke is used as test aerosol and the number concentration of particles > 0.3 µm is measured using an optical aerosol spectrometer usage of the indoor air cleaner (kAC). The decay rates k is determined from the measured temporal decay of the particle concentration C(t), starting from the initial concentration C0:. * Room size is calculated according to NRCC-54013 standard using CADR tested according to GB/T18801-2015.. NRCC: Method for Testing Air Cleaners. Formula for room size: Room size = 0.26*CADR. Note: The performance results may vary depending on the actual use environment of customers.

¹ Coway air purifiers has been proven to trap dust, pollen, dander, viruses, and bacteria in the air based on KCL (Korea Conformity Laboratories) testing. They have been tested in a 30㎥-size chamber according to the Korea Air Cleaning Association standard (SPS-KACA 002-132:2018 Modified) to measure the 0.01㎛ size of particle removal rate. It was tested on maximum fan speed in normal room temperature and humidity conditions. The performance may vary in the actual living environment of customers.. ² 99.9% of viruses, bacteria, fungi, and pollen were verified to be removed from the air by Coway air purifiers with GreenHEPA™ technology applied filters based on the Japan Food Research Laboratories (JFRL) testing according to JEM 1467 standard. Tested with AIRMEGA AP-1516D, AIRMEGA AP-1220B, AIRMEGA MIGHTY air purifiers and additionally AIRMEGA 150, AIRMEGA 250, AIRMEGA 300S, AIRMEGA 400S will acquire the test report in 1H, 2022.. All tested by JFRL and received above result within below time.. Virus: Tested with Escherichia coli phage ΦX174 NBRC 103405, 60 minutes. Bacteria: Tested with Staphylococcus epidermidis NBRC 12993, 60 minutes. Fungi/Mold: Tested with Penicillium citrinum NBRC 6352, 60 minutes. Pollen: Tested with Cedar Pollen extract, 30 minutes. Tested with Influenza A virus (H1N1) and Staphylococcus aureus on Coway’s Green HEPA filter media by Japan Food Research Laboratories (JFRL) and no growth was found on the material after 24 hours kept in room temperature.. Both tests were performed on small test pieces cut from the Green HEPA filter media, so this disclaimer can be used for any Coway products that use this filter.. Virus: Tested with Influenza A virus (H1N1), 3cm x 3cm autoclaved piece. Bacteria: Staphylococcus aureus, inoculated on 50mm x 50mm test piece.. ³ Tested with Human Coronavirus (HCoV-OC43) on Coway GreenHEPA™ technology applied filter media by BioPS Co., Ltd, a research organization specializing in viral clearance studies in South Korea. The test method was a filter media coupon test to observe the neutralization effectiveness. After 2 hours kept in room temperature, there was above 99.999% removal rate of the virus after the virus made contact with the filter media resulting in neutralization or inactivation of the virus is valid. Same result shows after 12 hours and 24 hours. This specific test was conducted with Human Coronavirus (HCoV-OC43) as the experimental model virus (Not Covid-19 (SARS-CoV-2)) because OC-43 is one of the seven types of Coronaviruses that can be infected to human.. Note: Air purifiers are known to be effective in preventing the Covid-19. However, it should never be regarded as the primary method of virus infection. Cleaning hands, trying to avoid contact and avoiding being in closed space in public is necessary to minimize the possibility of being affected by possible virus infection. Coway supports every patient and medical staff around the world who work tirelessly to prevent and cure the spread of hazardous viruses.. * CADR (Clean Air Delivery Rate) of particulate matter is tested according to GB/T18801-2015 by a certified third-party lab.. Measurement specifications are defined in GB/T 18801-2015, according to which two particle concentration decay rates have to be determined within a test chamber with a defined volume (Vchamber): a natural decay rate with inactive air cleaner (knat) and a decay rate detected under the measurements are carried out in a 30 ㎥chamber, which is empty except for the air cleaner placed on a table, two fans to mix and recirculate the air and some measurement periphery (mainly tubing). The chamber is kept at a temperature of 25 ± 2°C and a relative humidity of 50 ± 10%. Cigarette smoke is used as test aerosol and the number concentration of particles > 0.3 µm is measured using an optical aerosol spectrometer usage of the indoor air cleaner (kAC). The decay rates k is determined from the measured temporal decay of the particle concentration C(t), starting from the initial concentration C0:. * Room size is calculated according to NRCC-54013 standard using CADR tested according to GB/T18801-2015.. NRCC: Method for Testing Air Cleaners. Formula for room size: Room size = 0.26*CADR. Note: The performance results may vary depending on the actual use environment of customers.

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¹ Coway air purifiers has been proven to trap dust, pollen, dander, viruses, and bacteria in the air based on KCL (Korea Conformity Laboratories) testing. They have been tested in a 30㎥-size chamber according to the Korea Air Cleaning Association standard (SPS-KACA 002-132:2018 Modified) to measure the 0.01㎛ size of particle removal rate. It was tested on maximum fan speed in normal room temperature and humidity conditions. The performance may vary in the actual living environment of customers.. ² 99.9% of viruses, bacteria, fungi, and pollen were verified to be removed from the air by Coway air purifiers with GreenHEPA™ technology applied filters based on the Japan Food Research Laboratories (JFRL) testing according to JEM 1467 standard. Tested with AIRMEGA AP-1516D, AIRMEGA AP-1220B, AIRMEGA MIGHTY air purifiers and additionally AIRMEGA 150, AIRMEGA 250, AIRMEGA 300S, AIRMEGA 400S will acquire the test report in 1H, 2022.. All tested by JFRL and received above result within below time.. Virus: Tested with Escherichia coli phage ΦX174 NBRC 103405, 60 minutes. Bacteria: Tested with Staphylococcus epidermidis NBRC 12993, 60 minutes. Fungi/Mold: Tested with Penicillium citrinum NBRC 6352, 60 minutes. Pollen: Tested with Cedar Pollen extract, 30 minutes. Tested with Influenza A virus (H1N1) and Staphylococcus aureus on Coway’s Green HEPA filter media by Japan Food Research Laboratories (JFRL) and no growth was found on the material after 24 hours kept in room temperature.. Both tests were performed on small test pieces cut from the Green HEPA filter media, so this disclaimer can be used for any Coway products that use this filter.. Virus: Tested with Influenza A virus (H1N1), 3cm x 3cm autoclaved piece. Bacteria: Staphylococcus aureus, inoculated on 50mm x 50mm test piece.. ³ Tested with Human Coronavirus (HCoV-OC43) on Coway GreenHEPA™ technology applied filter media by BioPS Co., Ltd, a research organization specializing in viral clearance studies in South Korea. The test method was a filter media coupon test to observe the neutralization effectiveness. After 2 hours kept in room temperature, there was above 99.999% removal rate of the virus after the virus made contact with the filter media resulting in neutralization or inactivation of the virus is valid. Same result shows after 12 hours and 24 hours. This specific test was conducted with Human Coronavirus (HCoV-OC43) as the experimental model virus (Not Covid-19 (SARS-CoV-2)) because OC-43 is one of the seven types of Coronaviruses that can be infected to human.. Note: Air purifiers are known to be effective in preventing the Covid-19. However, it should never be regarded as the primary method of virus infection. Cleaning hands, trying to avoid contact and avoiding being in closed space in public is necessary to minimize the possibility of being affected by possible virus infection. Coway supports every patient and medical staff around the world who work tirelessly to prevent and cure the spread of hazardous viruses.. * CADR (Clean Air Delivery Rate) of particulate matter is tested according to GB/T18801-2015 by a certified third-party lab.. Measurement specifications are defined in GB/T 18801-2015, according to which two particle concentration decay rates have to be determined within a test chamber with a defined volume (Vchamber): a natural decay rate with inactive air cleaner (knat) and a decay rate detected under the measurements are carried out in a 30 ㎥chamber, which is empty except for the air cleaner placed on a table, two fans to mix and recirculate the air and some measurement periphery (mainly tubing). The chamber is kept at a temperature of 25 ± 2°C and a relative humidity of 50 ± 10%. Cigarette smoke is used as test aerosol and the number concentration of particles > 0.3 µm is measured using an optical aerosol spectrometer usage of the indoor air cleaner (kAC). The decay rates k is determined from the measured temporal decay of the particle concentration C(t), starting from the initial concentration C0:. * Room size is calculated according to NRCC-54013 standard using CADR tested according to GB/T18801-2015.. NRCC: Method for Testing Air Cleaners. Formula for room size: Room size = 0.26*CADR. Note: The performance results may vary depending on the actual use environment of customers.

Coway-luchtreinigers zijn bewezen effectief in het opvangen van stof, pollen, huidschilfers, virussen en bacteriën in de lucht op basis van testen door KCL (Korea Conformity Laboratories). Ze zijn getest in een kamer van 30㎥ volgens de standaard van de Korea Air Cleaning Association (SPS-KACA 002-132:2018 Aangepast) om het verwijderingspercentage van deeltjes van 0,01㎛ te meten. De test werd uitgevoerd op maximale ventilatorsnelheid onder normale kameromstandigheden qua temperatuur en luchtvochtigheid. De prestaties kunnen variëren in de daadwerkelijke leefomgeving van klanten. ² 99,9% van de virussen, bacteriën, schimmels en pollen zijn geverifieerd verwijderd uit de lucht door Coway-luchtreinigers met filters met toegepaste GreenHEPA™-technologie, op basis van testen door de Japan Food Research Laboratories (JFRL) volgens de JEM 1467-standaard. Getest met AIRMEGA AP-1516D, AIRMEGA AP-1220B, AIRMEGA MIGHTY luchtreinigers, en aanvullend zullen AIRMEGA 150, AIRMEGA 250, AIRMEGA 300S en AIRMEGA 400S het testrapport verkrijgen in het eerste halfjaar van 2022. Alle tests zijn uitgevoerd door JFRL en behaalden bovenstaande resultaten binnen onderstaande tijd: Virus: Getest met Escherichia coli-fage ΦX174 NBRC 103405, 60 minutenBacterie: Getest met Staphylococcus epidermidis NBRC 12993, 60 minutenSchimmel: Getest met Penicillium citrinum NBRC 6352, 60 minutenPollen: Getest met cederpollenextract, 30 minuten Getest met het Influenza A-virus (H1N1) en Staphylococcus aureus op Coway’s Green HEPA-filtermateriaal door Japan Food Research Laboratories (JFRL), en er werd geen groei aangetroffen op het materiaal na 24 uur bij kamertemperatuur. Beide tests zijn uitgevoerd op kleine teststukjes gesneden uit het Green HEPA-filtermateriaal, waardoor deze disclaimer van toepassing is op alle Coway-producten die dit filter gebruiken. Virus: Getest met Influenza A-virus (H1N1), 3 cm x 3 cm gesteriliseerd teststukBacterie: Staphylococcus aureus, aangebracht op een teststuk van 50 mm x 50 mm ³ Getest met humaan coronavirus (HCoV-OC43) op Coway GreenHEPA™-technologie toegepast filtermateriaal door BioPS Co., Ltd, een onderzoeksorganisatie gespecialiseerd in virusverwijderingsstudies in Zuid-Korea. De testmethode was een coupon-test op filtermateriaal om de effectiviteit van neutralisatie te observeren. Na 2 uur bij kamertemperatuur werd een verwijderingspercentage van meer dan 99,999% van het virus vastgesteld nadat het virus in contact was gekomen met het filtermateriaal, wat resulteerde in neutralisatie of inactivatie van het virus. Hetzelfde resultaat werd waargenomen na 12 uur en 24 uur. Deze specifieke test is uitgevoerd met humaan coronavirus (HCoV-OC43) als experimenteel modelvirus (niet Covid-19 (SARS-CoV-2)), omdat OC-43 een van de zeven typen coronavirussen is die mensen kunnen infecteren. Opmerking: luchtreinigers staan erom bekend effectief te zijn bij het voorkomen van Covid-19. Ze mogen echter nooit worden beschouwd als de primaire methode om virusinfectie te voorkomen. Handen wassen, contact vermijden en het vermijden van gesloten openbare ruimtes is noodzakelijk om de kans op besmetting met een mogelijk virus te minimaliseren. Coway ondersteunt elke patiënt en elk medisch personeelslid wereldwijd die onvermoeibaar werken om de verspreiding van gevaarlijke virussen te voorkomen en te behandelen. De CADR (Clean Air Delivery Rate) van fijnstof is getest volgens GB/T18801-2015 door een gecertificeerd extern laboratorium. Testspecificaties zijn gedefinieerd in GB/T 18801-2015, volgens welke twee vervalsnelheden van de deeltjesconcentratie moeten worden vastgesteld binnen een testkamer met een gedefinieerd volume (Vkamer): een natuurlijke vervalsnelheid met inactieve luchtreiniger (knat) en een vervalsnelheid gemeten tijdens gebruik van de luchtreiniger (kAC). De metingen zijn uitgevoerd in een kamer van 30㎥, die leeg is behalve de luchtreiniger geplaatst op een tafel, twee ventilatoren om de lucht te mengen en recirculeren, en meetapparatuur (voornamelijk leidingen). De kamer werd gehouden op een temperatuur van 25 ± 2 °C en een relatieve luchtvochtigheid van 50 ± 10 %. Sigarettenrook werd gebruikt als testaërosol en de deeltjesconcentratie > 0,3 µm werd gemeten met behulp van een optische aërosolspectrometer. De kamergrootte is berekend volgens de NRCC-54013-standaard met behulp van de CADR getest volgens GB/T18801-2015. NRCC: Methode voor het testen van luchtreinigersFormule voor kamergrootte: Kamergrootte = 0,26 × CADR Opmerking: de prestatie-resultaten kunnen variëren afhankelijk van de werkelijke gebruiksomgeving van klanten.