10 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DISPOSABLE MONOPOLAR NEEDLE ELECTRODE, VAR MODELS
FDA 510(k)
FDA Class 2
·Physical Medicine
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450252055·
SYRINGE 50ML LL AMBER
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·March 5, 2021
M VISUM ALERT ALARM MANAGEMENT SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
STERILE POWDER FREE SYNTHETIC VINYL PATIENT EXAM GLOVE
FDA 510(k)
FDA Class 1
·General Hospital
GEMSTAR 7 THERAPY S
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·May 13, 2014
INTRALASE
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code HNO·January 11, 2013
HARMONIC ACE 36CM W ERG HANDLE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·December 2, 2010
smiths medical Pneupac paraPAC plus 300 ventilator kit without PEEP and CPAP, REF P300NUS
FDA Enforcement
Class I
·Ongoing·Smiths Medical ASD Inc.·March 27, 2024
paraPAC 300 ventilator kit without internal PEEP and CPAP, Item Number P300N
FDA Enforcement
Class I
·Ongoing·Smiths Medical ASD Inc.·October 2, 2024