69 results
·
22ms
·
Sources: EU EUDAMED, US FDA
TEM 3000 HEAD COIL
FDA 510(k)
FDA Class 2
·Radiology
York 4 Trolley
FDA UDI
FERNO-WASHINGTON, INC.·00190790000455·York 4 Trolley, ship w/wheels off
econom® Vac. 2.7 V / XL 2.5 V,
FDA UDI
Rudolf Riester GmbH·04045396130593·The Riester otoscope is produced for illuminati...
JOBST forMen
FDA UDI
BSN MEDICAL, INC.·04042809849936·FOR MEN 15-20 MM HG KNEE HIGH OPEN TOE SMALL NA...
Mariner Outrigger
FDA UDI
Seaspine Orthopedics Corporation·10889981173890·L Con, Side-Loading, R, 16mm, 200mm
CAPELLA
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
1.5T INFINITY TWINSPEED MR SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
NUVASIVE
FDA Adverse Event
Injury
·NUVASIVE·Product code NKB·January 10, 2011
ARCHITECT CA19-9XR
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·October 31, 2025
ALINITY I CA 19-9XR REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·May 19, 2026
ACTIVA
FDA Adverse Event
Injury
·NEURO - VILLALBA·Product code MHY·April 11, 2013
XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code NIQ·April 12, 2011
FLORENCE BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL QUEBEC, LP·Product code FNL·May 21, 2008
ALINITY I CA 19-9XR REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·May 1, 2026
QUILL SRS
FDA Adverse Event
Other
·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·August 24, 2009
ALINITY I CA 19-9XR REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·May 14, 2026
ALINITY I CA 19-9XR REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·December 9, 2025
ARCHITECT CA19-9XR
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·December 22, 2025
ARCHITECT CA19-9XR
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·April 3, 2026
ALINITY I CA 19-9XR REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·November 4, 2025