10 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Viral Transport Media (VTM)
FDA 510(k)
FDA Class 1
·Microbiology
SILHOUETTE(TM) IC OR SILHOUETTE(TM) & LASER-LOK (TM)
FDA 510(k)
FDA Class 2
·Dental
VITAHEAT PATIENT WARMING SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
PAXGENE BLOOD CCFDNA TUBE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·July 13, 2021
PORTEX SOFT SEAL CUFF ENDOTRACHEAL TUBE
FDA Adverse Event
Malfunction
·SMITHS MEDICAL MD, INC.·Product code BTR·October 24, 2014
COLLEAGUE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 2, 2011
FLOGARD
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 18, 2013
BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·February 9, 2026
BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·February 10, 2026
BD VERITOR¿ PLUS ANALYZER
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code PSZ·March 7, 2025