The Purvigor KN95 Mask is made in an FDA Registered facility using the highest international manufacturing standards with CE Certification.
- FDA Registered Manufacturing
- CE Certified Manufacturing Standards
- Antibacterial Layer
- Pm 2.5 Standard
- Non-Woven Filtration Layer
- Dust Particle Protection
- Soft And Comfortable
Filtering facepiece respirators (FFR), which are sometimes called disposable respirators, are subject to various regulatory standards around the world.
These standards specify certain required physical properties and performance characteristics in order for respirators to claim compliance with the particular standard.
During pandemic or emergency situations, health authorities often reference these standards when making respirator recommendations, stating, for example, that certain populations should use an “N95, FFP2, or equivalent” respirator.
FFR performance standards:
• N95 (United States NIOSH-42CFR84)
• KN95 (China GB2626-2006)
• FFP2 (Europe EN 149-2001)
• P2 (Australia/New Zealand AS/NZA 1716:2012)
• Korea 1st class (Korea KMOEL – 2017-64)
• DS (Japan JMHLW-Notification 214, 2018)
Respirators certified as meeting these standards can be expected to function very similarly to one another, based on the performance requirements stated in the standards and confirmed during conformity testing.