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Personal Protective Equipment (PPE) Testing

The Food and Drug Administration (FDA), Centers for Disease Control and Prevention (CDC), and World Health Organization (WHO) have recently updated their guidelines to ensure Personal Protective Equiptment (PPE) can get to market faster. By issuing new guidance on testing and production for hand sanitizers, medical and consumer masks, medical gowns, and face shields, companies outside of the regularly licensed producers are now helping fill the unprecedented need for PPE.

Element has developed solutions to perform and/or coordinate the required testing for PPE, hand sanitizers, masks, gowns, and face shields, to ASTM F2100, USP 611, and ANSI Z87 standards to help you achieve the certification necessary to get these critical products into the hands of those who need them. 

Hand Sanitizer Testing

Following the CDC and World Health Organization’s policy, all hand sanitizers in production are required to undergo USP 611 Method II: Alcohol Determination performed by GC-FID before they can be released to the market.

Element offers alcohol determination testing by GC-FID per USP 611 to verify that at least 70% isopropyl alcohol (IPA) or 60% ethanol is present in the product. Our GC-FID method is the most precise and cost-effective of the methods allowed under USP 611 because it allows direct analysis of the sample matrix. This direct analysis allows our experts to quantify the ethanol or IPA present in the product without extensive sample preparation, reducing your testing cost while providing more precise results.

Element also offers alcohol determination testing by GC-MS to identify any additional compounds that may be present in the product and could be harmful to users.

Our Santa Fe Springs Pharma laboratory can also provide testing of ethanol and isopropyl alcohol against the USP monograph specifications as raw materials intended for use in the manufacturing of hand sanitizer products under US FDA guidelines.

We offer expedited service when needed for alcohol content identification testing.

Medical and Consumer Face Mask Testing

Per FDA guidelines, medical face masks are required to undergo testing per ASTM F2100 methods before they can be distributed for use. Testing also needs to consider the intended use and applicability of the test methods for the desired regulatory submission. Consumer masks only require method 9.5, but methods 9.2 and 9.3 are highly encouraged to verify mask effectiveness. 

Element is one of the few testing laboratories that can facilitate all five methods. Our experts can guide you through the process and provide one complete testing report for medical masks.

  • Method 9.1 – ASTM F2101 – Bacterial Filtration
  • Method 9.2 – EN 14683:2019 – Differential Pressure
  • Method 9.3 – ASTM F2299 – Particulate Filtration
  • Method 9.4 – ASTM F1962 – Synthetic Blood
  • Method 9.5 – 16 CFR Part 1610 - Flammability 

While N95 masks are traditionally single-use, the unprecedented shortage has resulted in decontamination efforts to re-use these devices. Element can perform residual hydrogen peroxide testing on new masks to ensure that the client procedure for decontamination does not leave behind residual H2O2.

Medical Gown Testing

Building and Fire Codes require all fabrics and films, including medical gowns, to undergo flame propagation testing before they can be released to the market. Because textiles and films provide a convenient conduit for flame spread, they can be significant contributors to the growth of building fires. Assessing their flammability characteristics is crucial to understand whether a fire is likely to start and how the flame will develop.

We offer a 2-3 day turn-around from receipt of samples for flame propagation testing for medical gowns by ASTM F2100 Method 9.5, CAN/ULC-S109, and NFPA 701 Methods 1 and 2 to ensure that medical gowns do not pose a fire hazard.

Face Shield Testing

Per American National Standards Institute (ANSI) guidelines, all face shields must undergo testing to the ISEA Z87.1-2020 specification to ensure safety and effectiveness in preventing eye and face injuries before they can be released to the market.

Element conducts the six critical sections of the specification to ensure the effectiveness of face shields in a medical environment. These sections include:

  • Section 5.2.4 – Minimum Coverage Area
  • Section 9.2 – Transmittance
  • Section 9.3 – Haze
  • Section 9.6 – Drop Ball
  • Section 9.7 – Ignition
  • Section 9.17.2 – Droplet and Splash

The Element Advantage

Element’s dedicated team of experts have years of experience in a wide range of testing services for the medical device and product certification industries to help you meet regulations and ensure that every aspect of your product is properly tested. 

For more information on personal protective equipment (PPE) testing, please contact us today.

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