206 results · 25ms · Sources: EU EUDAMED, 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