25 results
·
27ms
·
Sources: EU EUDAMED, US FDA
ELECSYS PROBNP IMMUNOASSAY
FDA 510(k)
FDA Class 2
·Clinical Chemistry
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526827943·ACHIMED ACHILLES SUPP BLACK VI
APEX PS Knee
FDA UDI
Omni Life Science, Inc.·00841690113744·PS-C Insert, Size 5 x 16mm
6mm Aspiration Kit
FDA UDI
MEDGYN PRODUCTS, INC.·M803022516·6mm Aspiration Kit
CARE IFC PLUS
FDA 510(k)
FDA Class 2
·Neurology
EBI SPINELINK - II SPINAL FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
DEXCOM FOLLOW APP
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·January 27, 2025
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0225168701315917201·BTE
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0225168701312717201·BTE
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0225168701312017201·BTE
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0225168701338117201·BTE
audifon
FDA UDI
audifon GmbH & Co. KG·EADF022516870133217201·BTE
audifon
FDA UDI
audifon GmbH & Co. KG·EADF022516870131217201·BTE
audifon
FDA UDI
audifon GmbH & Co. KG·EADF022516870132517201·BTE
audifon
FDA UDI
audifon GmbH & Co. KG·EADF022516870131317201·BTE
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0225168701338217201·BTE
DRILL, 2.75MM, .066 CANNULATION
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MDM·October 27, 2025
COTTON-LEUNG BILIARY STENT
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·March 20, 2013
INRATIO
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·February 15, 2011
ACCU-CHEK COMPLETE
FDA Adverse Event
Injury
·ROCHE DIAGNOSTICS·Product code NBW·April 1, 2008