Some products with legitimate manufacturer names, showing poor filter penetration results (<95%), are counterfeit products. Indicators of Fraudulent or Counterfeit Vendors/Suppliers The Indicators of Fraudulent 3M Personal Protective Equipment Liaison Information Report, prepared by the FBI and 3M, highlights the following tactics commonly used by criminals: Demand up-front payment of all or a … Shandong Daddy’s Choice Health Science and Technology Co., Ltd. Shandong Haidike Medical Products Co., Ltd. Shandong Minghang Nonwoven Products Co., Ltd. Shandong Shengquan New Materials Co., Ltd. Biomass Graphene Particulate Respirator (C-Shaped), Biomass Graphene Particulate Respirator (Willow leaf-Shaped). He will issue the certificate on the final day of the course. Location: This program is usually held at a local hotel, located between … No … NIOSH-Approved Particulate Filtering Facepiece Respirators. over suppliers and distributors of respirators certified by other national or international parties. The test articles submitted by the sponsor conform to this criterion for airflow resistance. The samples were tested using the modified version of NIOSH Standard Test … Further, no certificates of approval were provided with the samples. ... Counterfeit respirators are products that are falsely marketed and sold as being NIOSH-approved and may not be capable of providing appropriate respiratory protection to workers. As part of its standard respirator approval process for NIOSH-approved respirators, NIOSH conducts a … Hunan Royal Crown Medical Products Co., Ltd. Medical Protective Mask (Non-Sterile) – Foldable Type, Hunan YuanKang Biological Technology Co, Ltd, Hunan Youhong Medical Technology Co., Ltd. Jiangmen Huadizhiguang Lighting Co., Ltd. JT-KN95 Reusable and Sterilizable Nano-mask KN95. Respirator Assessment Results Considered as Counterfeit and/or Misuse of Company Name, Centers for Disease Control and Prevention. The results of these tests are for the sample tested and may or may not be representative of a larger lot or population of similar respirators. The ‘KN95’ types present pressure drops which correspond to the … Therefore, validation of the claims that the product meets a particular international standard cannot be made. CDC is not responsible for Section 508 compliance (accessibility) on other federal or private website. Total inward leakage is defined as the combination of contaminated air that … This was certainly a record year for NIOSH … Explore AIHA. This guidance provides Crisis Alternate Strategies that includes the option: “Use of respirators approved under standards used in other countries that are similar to NIOSH-approved N95 respirators.” The other countries listed in the guidance and their associated product classifications are shown below. “I encourage everyone to not just focus on the filtration efficiency numbers, but to really look at the reports,” Powers told webinar … • This assessment is not a confirmation that it conforms with any or all of its specifications in accordance with its certification mark. Students who successfully complete the USF/COPH NIOSH-approved spirometry training course will receive a certificate from Dr. Thomas Truncale. The laboratory evaluated filtration performance of more than 8,500 respirators during the COVID-19 response, resulting in 550 reports informing the use of respirators that were 1) conforming to international … NPPTL has recently received new information from Stakeholders across the United States regarding products from China claiming to meet GB2626 and EN149. While the above-listed product classification has similar performance requirements to NIOSH-approved devices, NIOSH does not have knowledge about the sustained manufacturer quality system and product quality control for these products. Due to heightened concerns over counterfeiting, NPPTL will require review and validation of emails lacking recognizable company or organizational domains. Do your safety and health job better … The results posted to the NIOSH website identify the manufacturer of the respirator, the model number or product line, the international standard the product claims to meet, and filtration efficiency. For each model listed, ten respirators were submitted for evaluation. Therefore, the authenticity of the claims, that the product meets a particular international standard, cannot be validated. Changshu City Hengyun Nonwoven Products Co., Ltd. Chongqing China Nano Technology Co., Ltd. Dongguan Angel Leather Technology Co. Ltd. Dongguan HuaGang Communication Technology Co., Ltd. Dongguan Liangji Technology Development Co., Ltd. Dongguan Oukangda Medical Technology Co., Ltd. Dongguan Sengtor Plastics Products Co., Ltd. Foldable Protective Earloop Mask Non-Medical, Dongguan Tian Ren He Yi intelligent Co., LTD. Dongguan Weicon Medical Equipment Technology Co., Ltd. Dongguan Wei Sheng Medical Technology Co., Ltd. Dongguan Xianda Medical Equipment Co., Ltd. Dongyang Qingdou Household Commodity Co., Ltd. Elizabeth (Guangzhou) Medical Technology Co., Ltd. Fengxian Ratone Medical Technology Co., Ltd. Foshan Daylead Newcon Technology Co., Ltd. Foshan Nanhai Weijian Sanbang Protective Equipment Technology Co., Ltd. Foshan Nanhai Weijian SanBang Protective Products Technology Co., Ltd. Fujian Jimei Household Products Co., Ltd. Fujian Little Forest Technology Co., Ltd. Fujian Sunkinetic Smart Technology Co., Ltd. N95 Particulate Respirator (non-medical mask). Guangdong Kaper Protection Technology Co., Ltd. Guangdong Mingxiang Medical Instrument Co., Ltd. Guangdong Nuokang Medical Technology Co., Ltd. Guangdong Shantou Haimeisi Clothing Co., LTD. Guangdong Zhizhen Biological Medicine Co., Ltd. KN95 Three-Dimensional Protective Respirator, KN95 Three-Dimensional Protective Respirator (disposable respirator). The exhalation resistance criteria as stated in 42 CFR Part 84.180 is an initial exhalation not exceeding 25 mm water column height pressure. Become an IH Hero. How to read a Flow - Volume display Learn how to recognize obstructive & restrictive patterns, hesitating starts, coughs, and other causes of poor subject effort that may invalidate test results. Linking to a non-federal website does not constitute an endorsement by CDC or any of its employees of the sponsors or the information and products presented on the website. All lectures are given by Dr. Roy McKay, who has taught this course for nearly three (3) decades. National Institute for Occupational Safety and Health (NIOSH)-approved respirators are required by the Occupational Safety and Health Administration (OSHA) when personal respiratory protection is used in US occupational settings. CDC’s Factors to Consider When Planning to Purchase Respirators from Another Country. It needs to be understood that product test results meeting the requirements of a single STP, TEB-APR-STP-0059 pdf icon, does not imply the respirator is NIOSH approved. performance assessments on some of the international FFRs available in the United States that are not NIOSH approved, and posts the results on its website.17 The postings include the name of the manufacturer, the model number, the international standard used to manufacture the respirator, the maximum and minimum filtration efficiency (%) results and a link to a copy of the complete test … NIOSH has been informed that many legitimate manufacturers in China have been counterfeited. Inspect the respirator and/or its packaging for the required labeling, as seen in the image above. The International Respirator Assessment is a point-of-use assessment and is not to be used by manufacturers, distributers, suppliers, or importers attempting to sell products in the United States. The Centers for Disease Control and Prevention (CDC) cannot attest to the accuracy of a non-federal website. NPPTL has completed International Assessments for the products listed below. Why not think of a mission-focused STEM career? Guangzhou Powecom Labor Insurance Supplies Co., Ltd. … Respirator Assessments to Support the COVID-19 Response, International Assessment Results . All submissions must include the respirator manufacturer, the model number/name, and verification of the standard that was used. To protect American workplaces, requests from federal and state agencies, employers, and healthcare systems will be accepted. The International Respirator Assessment requires that 10 samples be sent. As part of its standard respirator approval process for NIOSH-approved respirators, NIOSH conducts a comprehensive quality assurance review of the quality process and manufacturing site. In such cases, NIOSH has no way of verifying which products are counterfeit and which are authentic. Filtering Efficiency Excerpted from International Assessment Results – Not NIOSH-approved as of September 1, 2020 Manufacturer. Check for inconsistent markings. International . This assessment is not a part of the NIOSH respirator approval process and will in no way lead to or preclude NIOSH approval through the official approval process. While the manufacturer listed in the table is shown as the manufacturer of the product evaluated, NIOSH has been informed that some of these are actually counterfeit products. During the COVID-19 pandemic, the demand for NIOSH-approved N95 filter … CDC's NPPTL Respirator International Assessments Filtration Results for not NIOSH-approved to determine if filtration levels are adequate for your use. A number of manufacturers have also informed NIOSH that they did not produce the products associated with their name. This assessment was developed as an assessment of the filter efficiency for those respirator’s represented as certified by a foreign certification authority, other than NIOSH, to support the availability of respiratory protection to US healthcare workers due to the respirator shortage associated with COVID-19. Guangdong Nafei Industrial Holding Co., Ltd. Guangzhou Kangbang Medical Equipment Co., Ltd. Guangzhou Kangling Medical Supplies Co., Ltd. Shenzhen Hangsen Star Technology Co., Ltd. These assessments are not a part of the NIOSH respirator approval process and will in no way lead to or preclude NIOSH approval through the official approval process. CDC's NPPTL Respirator International Assessments Filtration Results for not NIOSH-approved to determine if filtration levels are adequate for your use. Assessment results confirm that some of these products have poor filter efficiency and are of poor quality. To protect American workplaces, requests from federal and state agencies, employers, and healthcare systems will be accepted. Our experienced staff works closely with NIOSH, … Shandong Sino Medical Equipment Co., Ltd. Shandong Tricol Marine Biological Technology Co., Ltd. Shandong Zhushi Pharmaceutical Group Co., Ltd. Shanghai Dasheng Health Products Manufacture Co., Ltd. Shanghai Gangkai Purifying Products Co., Ltd. Shanghai Huaxiang Woolen Dressing Co., Ltd. Shanghai Kindly Medical Instruments Automation Research Center Co., Ltd. Shenzhen Dingwei Optical Technology Co., Ltd. Shenzhen FITTOP Health Technology Co., Ltd. Shenzhen Guidong Information Consulting Co., Ltd. Shenzhen Jiameilantai Industrial Co., Ltd. Shenzhen Kawang Network Technology Co., Ltd. Shenzhen Mingjiang Medical Supplies Development Co., Ltd. Shenzhen Sanai Medical Devices Group Co., Ltd. SHENZHEN XIANDA INFORMATION TECHNOLOGY CO., LTD. Shenzhen Zhanhuwei Medical Supplies Co., Ltd. Shenzhen Zhongyue Health Technology Co., Ltd. Suzhou Jinruida Protective Equipment Co, Inc. Suzhou Letian Protective Products Co., Ltd. TF-003 Effective Particles Filtering Mask. NIOSH-approved N95s typically have head bands. These results are not to be used by manufacturers, distributors, suppliers, and importers to make claims about their products and/or to influence purchasers. • Assessment of Filter Penetration Performance for Non-NIOSH Approved Respirators – NPPTL Assessment to Support the COVID-19 Response (10 samples) Modified TEB … NIOSH-approved N95s typically have head bands. None of these reviews were conducted during this limited assessment. AIHA is here to help you and your loved ones stay healthy at work and in your community. This course uses a combination of lectures and hands-on practice … Before proceeding to the form below, please check the International Respirator Assessment Results to see if we have already assessed the product you have. Saving Lives, Protecting People, The National Personal Protective Technology Laboratory (NPPTL), Strategies for Optimizing the Supply of N95 Respirators, CDC Strategies for Optimizing the Supply of N95 Respirators: Crisis/Alternate Strategies, National Institute for Occupational Safety and Health, Filtering out Confusion: Frequently Asked Questions about Respiratory Protection, Respirator Assessments to Support COVID-19 Response, Beyond Shelf Life/Stockpiled Respirator Assessment Request, Beyond Shelf Life/Stockpiled Assessment Results, International Respirator Assessment Request, Decontaminated Respirator Assessment Request, Non-NIOSH approved Innovative Filtering Facepiece Respirator Assessment Request, Decontaminated International Respirators Assessment Request, Healthcare Respiratory Protection Resource, Support for Firefighter Personal Protective Equipment, Participation on Standards Setting Organizations, Considerations for Selecting Protective Clothing, NPPTL Participation in Standard Development Committees, Section 3: Ancillary Respirator Information, Additional Respiratory Protection Resources, Approved Particulate Filtering Facepiece Respirators, Conformity Assessment Notices and Letters to Respirator Manufacturers and Interested Parties, U.S. Department of Health & Human Services. The International Respirator Assessment is a point-of-use assessment and is not to be used by manufacturers, distributers, suppliers, or importers attempting to sell products in the United States.