25 results
·
47ms
·
Sources: EU EUDAMED, US FDA
Niox Vero (FeNO device)
FDA registration
TURNKEY EXPORT COMPLIANCE BV·1 product·🇳🇱 Netherlands
5F DIGNITY CT TITANIUM PORT
FDA 510(k)
FDA Class 2
·General Hospital
COBAS 4800 CT / NG TEST
FDA 510(k)
FDA Class 1
·Microbiology
Dna Probe, Nucleic Acid Amplification, Chlamydia
FDA classification
FDA Class 1
·Dna Probe, Nucleic Acid Amplification, Chlamydia
Port & Catheter, Implanted, Subcutaneous, Intravascular
FDA classification
FDA Class 2
·Port & Catheter, Implanted, Subcutaneous, Intravascular