Surgical Mask and N95 Respirator Testing
Project Description
MULTIPLE TESTS
MULTIPLE PRODUCTS
CONTRACT LABORATORY NEEDED FOR MULTIPLE TESTS ON SURGICAL MASKS AND NIOSH PRE-TESTS FOR N95 RESPIRATORS
SURGICAL MASKS:
- Bacterial Filtration Efficiency (BFE) Method reference: EN 14683:2019+AC:2019 Annex B Method: ASTM F2101
- Determination of face mask materials efficiency to penetration by particulates (latex spheres) Method reference: ASTM F2299 / F2299M - 03(2017)
- Breathability (Differential Pressure) (A) Method reference: ASTM F2100 - 19e1 Sec.9.2 / EN 14683:2019+AC:2019 Annex C
- Resistance to penetration by synthetic blood tested to P= 120 mmHg (A) Method reference: ASTM F1862/F1862M - 17 / ASTM F2100 - 19e1 Sec.9.4
- Flammability (A) 576.00 1 576.00 Method reference: 16 CFR 1610:2019
- Biocompatibility
N95: NIOSH PRE-TESTS
Project Information
Number:21-00678
Industry:Medical Devices
Other medical devices laboratory services.
Other Medical Devices testing, analysis, scientific research and development, inspection, certification, engineering, failure investigation, and product development needs include :
- Biomaterials Testing
- of Tissues Testing
- Bone and Joint Computer Modeling Testing
- Ethylene Oxide Biological Indicators Performance Testing
- GHG Emissions Testing
- Implantable Medical Device Testing
- In-Vitro Diagnostic Testing
- Precision Testing
- Sensitivity Testing
- Specificity Testing
- Medical Device AATCC and ASTM Antimicrobial Testing
- Medical Device ASTM Extractable Testing
- Medical Device Barrier Testing
- Medical Device Bioburden Testing
- Total Aerobes Testing
- Total Coliforms Testing
- Total Fungi Testing
- Medical Device Biodegradation Subchronic Toxicity Studies Testing
- Medical Device Biomaterial Extracts Protein Assays Testing
- Medical Device Carcinogenicity Testing
- Medical Device Compliance Testing
- Medical Device Container/Closure Testing
- Medical Device Contamination Testing
- Medical Device Design and Modeling of Systems Medical Device Environmental Monitoring Testing
- Medical Device Ex-Vivo Hemocompatibility Studies Medical Device Finished Product Quality Control Testing
- Medical Device Genotoxicity Ames Testing
- Medical Device Genotoxicity Chromosomal Aberration Testing
- Medical Device Histopathology Testing
- Medical Device ISO 10993-1 (FDA GP 95-1) Biological Safety Testing
- Medical Device In-Vitro Biocompatibility Studies Testing
- Medical Device In-Vivo Biocompatibility Studies Medical Device In-Vivo Hemocompatibility Studies Testing
- Medical Device Irritation Studies Testing
- Medical Device Leachable Testing
- Medical Device Microbial Identifications Testing
- Medical Device Mutagenicity Testing
- Medical Device Particles Analysis Testing
- Medical Device Particulate Testing
- Medical Device Physical Testing
- Medical Device Preclinical Testing
- Medical Device Product Inoculations Testing
- Medical Device Product Safety Testing
- Medical Device Radiological Testing
- Medical Device Sensitization Testing
- Medical Device Shipping Validations and Shipping Testing
- Medical Devices Impact Resistance Testing
- Simulated Use Testing
- Medical Device Stability Studies Testing
- Medical Devices Accelerated Aging Stability Studies Medical Devices Real Time Stability Studies Medical Device Sterility Testing
- Medical Device Sterilization Dose Validation Medical Device Sterilization Validation Medical Device Tensile Testing
- Medical Device Thermal Analysis Testing
- Medical Device USP Implantation Studies Medical Device USP Microbial Limits Testing
- Medical Device USP and EP Plastics and Container Testing
- Medical Device USP Glass Container Testing
- Medical Device USP Polyethylene Container Testing
- Medical Device USP Testing
- AAMI Testing
- EP Bacteriostasis/Fungistasis Testing
- Medical Devices Analytical Chemistry Testing
- Medical Devices Bacterial Endotoxin Testing
- - Gel Clot Testing
- Medical Devices Bacterial Endotoxin Testing
- - Limulus Amebocyte Lysate LAL Testing
- Medical Devices Biomaterials Testing
- Medical Devices Biomechanical Platform Testing
- Medical Devices Biomechanical Testing
- Medical Devices Biomedical Testing
- Medical Devices Biomedical Testing
- Medical Devices Biophysical Characterization Testing
- Medical Devices Biophysical Properties Testing
- Medical Devices Biophysical Testing
- Medical Devices Cleaning Validation Testing
- Medical Devices Conformity Assessments Testing
- Medical Devices Cytotoxicity Testing
- Medical Devices Electrical Safety Testing
- Medical Devices Electromagnetic Compatibility Testing
- EMC Testing
- Medical Devices Ethylene Oxide Residuals Testing
- Medical Devices Failure Analysis Testing
- Medical Devices Fatigue Testing
- Medical Devices Fatigue Testing
- Medical Devices Foreign Materials Testing
- Medical Devices In-Vivo USP Testing
- JP Testing
- EP Pyrogen Testing
- Medical Devices Leak Testing
- Medical Devices Materials Characterization Testing
- Medical Devices Methods Development and Validation Testing
- Medical Devices Microbiology Testing
- Medical Devices Packaging Studies and Testing
- Medical Device Package Integrity Testing
- Medical Device Packaging Burst Testing
- Medical Device Packaging Creep Testing
- Medical Device Packaging Dye Penetration Testing
- Medical Device Packaging Peel Testing
- Medical Device Packaging Vacuum Leak Testing
- Medical Devices Safety Evaluations Testing
- Medical Devices Toxicology Testing
- Medical Devices Transportation Simulation Testing
- Medical Devices Vibration Testing
- Medical Products Re-engineering Testing
- Medical Products Reverse Engineering Testing
- Reusable Device Studies Testing
- Reusable Medical Devices Testing
- RoHS Testing
- Steam Biological Indicators Performance Testing
- USP Purified Water Testing
- USP Water for Injection Testing
- WEEE Testing