11 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
×
OraQuick Ebola Rapid Antigen Test
FDA 510(k)
FDA Class 2
·Microbiology
Device To Detect Antigens Of Biothreat Microbial Agents In Human Clinical Specimens
FDA classification
FDA Class 2
·Device To Detect Antigens Of Biothreat Microbial Agents In Human Clinical Specimens
FilmArray Respiratory Panel 2 plus (RP2plus)
FDA 510(k)
FDA Class 2
·Pathology
BioFire Global Fever Special Pathogens Panel; BIOFIRE SHIELD Control Kit for the BioFire Global Fever Special Pathogens Panel
FDA 510(k)
FDA Class 2
·Immunology
T2 Biothreat Panel
FDA 510(k)
FDA Class 2
·Immunology
FilmArray Pneumonia Panel plus
FDA 510(k)
FDA Class 2
·Pathology
BIOFIRE® FILMARRAY® Pneumonia Panel (BIOFIRE Pneumonia Panel); BIOFIRE® FILMARRAY® Pneumonia Panel plus (BIOFIRE Pneumonia Panel plus)
FDA 510(k)
FDA Class 2
·Pathology
FilmArray Pneumonia Panel plus
FDA 510(k)
FDA Class 2
·Pathology
Multiplex Nucleic Acid Detection System For Biothreat Agents
FDA classification
FDA Class 2
·Multiplex Nucleic Acid Detection System For Biothreat Agents
Mers-Cov And Common Respiratory Pathogens Multiplex Nucleic Acid Detection System
FDA classification
FDA Class 2
·Mers-Cov And Common Respiratory Pathogens Multiplex Nucleic Acid Detection System
Mers-Cov And Common Respiratory Pathogens Semi-Quantitative And Quantitative Multiplex Nucleic Acid Detection System
FDA classification
FDA Class 2
·Mers-Cov And Common Respiratory Pathogens Semi-Quantitative And Quantitative Multiplex Nucleic Acid Detection System