259 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
ANCHOR
FDA Adverse Event
Malfunction
·BAXTER SURGICAL·Product code EJX·June 9, 1992
Anchor, Preformed
FDA classification
FDA Class 1
·Anchor, Preformed
Elx
FDA UDI
Drive Devilbiss Healthcare·00822383508344·Elx, Pacifica Elite Neb
NORDENT MANUFACTURING INC
FDA UDI
NORDENT MANUFACTURING INC·00840018639515·ELEVATOR POTTS #6 X-BAR HANDLE
HU-FRIEDY
FDA UDI
HU-FRIEDY MFG. CO., LLC·10889950009304·#6X Potts T-Bar Elevator
Economy Apron
FDA UDI
Shielding International Inc.·G031E2XRL0·Economy Coat Apron - XX-Large 0.5mm Regular...
EyeBOX EBX-4.1
FDA 510(k)
FDA Class 2
·Neurology
EyeBOX (Model EBX-4)
FDA 510(k)
FDA Class 2
·Neurology
William's Medium E (1X)
FDA UDI
LIFE TECHNOLOGIES CORPORATION·10190302002431·
Bipolar Cable
FDA UDI
SONIQUENCE, LLC·00810026181757·Bipolar Cable, Sterile/Disposable
Philips IntelliVue GuardianSoftware (Rev. E.0X)
FDA 510(k)
FDA Class 2
·Cardiovascular
KING OF HEARTS EXPRESS (E.X.) MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
Lead Test Adaptor, remede EL-X
FDA UDI
RESPICARDIA, INC.·00857688007421·Lead Test Adaptor, remede EL-X, for use with In...
remede EL/EL-X External Pulse Generator
FDA UDI
RESPICARDIA, INC.·00857688007414·remede EL/EL-X external pulse generator
FLEXIVA (TM) HIGH POWER SINGLE-USE LASER FIBER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code GEX·September 11, 2014
FLEXIVA (TM) HIGH POWER SINGLE-USE LASER FIBER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code GEX·January 8, 2016
WECK EFX
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code GCJ·September 15, 2014
NICOLET EDX
FDA Adverse Event
Malfunction
·NATUS NEURO INCORPORATED·Product code GWF·April 10, 2019
WECK EFX
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code GCJ·September 6, 2013
VIKING EDX
FDA Adverse Event
Injury
·NATUS NEUROLOGY INCORPORATED·Product code GWF·July 8, 2013