- Particle Filtration Efficiency (PFE): >= 99.9%
- Viral Filtration Efficiency (VFE): >= 99.9%
- Fluid Resistance: Resists Synthetic Blood @160mmHg of pressure
- Conforms with KMOEL-2017-64 KF94 (Korea Standards)
- Passed NIOSH 42 CFR 84 N95 filtration test (US)
- Conforms with ASTM F2100-19 Level 3 (US Standards)
- Conforms with EN14683:2019 TYPE IIR (EU Standards)
- Conforms with JIS T 9001:2021 Class III (Tested by KAKEN)
- Passed the ISO10993-10 Skin Irritation and Sensitization Test
- Passed the ISO10993-5 Minimal Essential Media (MEM) Elution Test
- Passed the Microbial Cleanliness (Bioburden) Test
- Latex free and antiallergic
- Does not contain 212 SVHC materials
- No Azo Dye in Textile
- Fluorescent-free, latex-free, hypoallergenic
- Produced at ISO14644-1 Class7 Cleanroom
- ISO13485:2016 Quality Management System for Medical Devices
- ISO14001-2015 Environmental Management System
- ISO9001-2015 Quality Management System
- CE Marking Certification (EU)
- KFDA Registration (KR), Registration No. 202107925
- FDA Registration (US), Registration No. 3017178899
- Design and manufactured in Hong Kong
- Individual packaging