206 results
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25ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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LIQUICHEK BLOOD GAS PLUS CO-OXIMETER CONTROL (IL SYNTHESIS SERIES) LEVELS 1,2, AND 3, MODELS 667,668,669
FDA 510(k)
FDA Class 1
·Clinical Chemistry
LARGE CENTRIFUGAL BLOOD PUMP, MODEL CP-2
FDA 510(k)
FDA Class 2
·Cardiovascular
ROK
FDA 510(k)
FDA Class 2
·Dental
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0225298708338117201·BTE
audifon
FDA UDI
audifon GmbH & Co. KG·EADF022529870833217201·BTE
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0225298708312717201·BTE
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0225298708315917201·BTE
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0225298708338217201·BTE
audifon
FDA UDI
audifon GmbH & Co. KG·EADF022529870832517201·BTE
audifon
FDA UDI
audifon GmbH & Co. KG·EADF022529870831217201·BTE
audifon
FDA UDI
audifon GmbH & Co. KG·EADF022529870831317201·BTE
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0225298708312017201·BTE
SURGICAL STAINLESS STEEL SUTURE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code GAO·March 27, 2013
MEDISENSE OPTIUM
FDA Adverse Event
Malfunction
·Product code NBW·March 17, 2011
VISIAN ICL (IMPLANTABLE COLLAMER LENS)
FDA Adverse Event
Other
·STAAR SURGICAL·Product code MTA·March 26, 2008
BD PHOENIX¿ NMIC-311
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 19, 2026
BD PHOENIX¿ NMIC-311
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 19, 2026
BD PHOENIX¿ NMIC-306
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 28, 2026
BD PHOENIX¿ NMIC-306
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 14, 2026
BD PHOENIX¿ NMIC-306
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026