Mandatory certification

EU Type-Examination Certificate –A certificate issued by the certifying body VÚBP in the Czech Republic, which certifies the product RespiRaptor as an FFP2 respirator with filtration efficiency for solid particles above 94%. The product meets the requirements of the European standard EN149:2001 + A1:2009.

EC declaration of Conformity – The declaration of conformity is issued by the manufacturer of the product. It informs about the fact that the product has been assessed to be in conformity with relevant standards and laws, is safe and used in compliance with the listed recommendations, standards, and laws.

Additional certification

Certificate GB2626 – The standard that is acceptable in China which states that RespiRaptor is classified as a FFP2 respirator.

Mandatory certification 

EU Type Examination Certificate –  A certificate issued by the certifying body GÉPTESZT in Hungary, which certifies the second generation of the product RespiPro White as an FFP2 respirator with filtration efficiency for solid particles above 94%. The product meets the requirements of the European standard EN149:2001 + A1:2009.

EC declaration of Conformity – The declaration of conformity is issued by the manufacturer of the product. It informs about the fact that the product has been assessed to be in conformity with relevant standards and laws, is safe and used in compliance with the listed recommendations, standards, and laws.

Additional certification

Test report on viral filtration efficiency – A test report issued by the American institute Nelson Labs which confirms that the filtration efficiency of viruses of the RNF 2.0 filtration nanofiber membrane used in the second generation of RespiPro White is 99.9%.

Test report on bacterial filtration efficiency – A test report issued by the American institute Nelson Labs which confirms that the filtration efficiency of bacteria of the RNF 2.0 filtration nanofiber membrane used in the second generation of RespiPro White is 99.9%.

Mandatory certification 

EU Type Examination Certificate – Certified by the certification body FORCE in Denmark, which tested the RespiPro White product and concluded that RespiPro White is in accordance with the recommendations for use (RFU), i.e., the filtration efficiency complies with the standard for respirators of RFU 02.075, version 2. The respirator is manufactured to protect against the coronavirus disease (COVID-19). As required by the recommendations of the World Health Organization for this specific purpose, the nominal filtration factor of the respirator is the same as the nominal filtration factor of FFP2 defined in EN149: 2001 + A1: 2009.

EC declaration of Conformity – The declaration of conformity is issued by the manufacturer of the product. It informs about the fact that the product has been assessed to be in conformity with relevant standards and laws, is safe and used in compliance with the listed recommendations, standards, and laws.

Additional certification

Test report on viral filtration efficiency – A test report issued by the American institute Nelson Labs which confirms that the filtration efficiency of viruses of the RFT filtration nanofiber membrane used in the RespiPro White product ranges between 99.7% up to 99.9%.

Test report in line with the Czech standard ČSN EN ISO 10993 assessing cytotoxicity, skin irritability and sensibilization – The National Institute of Public Health in Prague, testing laboratory nr. 1206, certified by the Czech Accreditation Institute, Centre of Toxicology and Health Safety tested RespiPro White in line with the Czech standard ČSN EN ISO 10993. The tests have shown that RespiPro White is not cytotoxic, is not a skin irritant and shows no skin sensibilization potential.